DailyMed - 4379 FIRST AID KIT kit 4334 FIRST AID KIT kit

NDC Code(s): 0498-0121-00, 0498-0143-04, 0498-0203-00, 0498-0501-00, view more
0498-0750-35, 0498-2110-01, 0498-4334-01, 0498-4379-01
Packager: Honeywell Safety Products USA, INC

Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated January 22, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

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Official Label (Printer Friendly)

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Triple Active ingredients

Bacitracin zinc 400 units

Neomycin sulfate (5 mg equivalent to 3.5 mg Neomycin base)

Polymyxin B sulfate 5000 units
Triple Purpose

First aid antibiotic

First aid antibiotic

First aid antibiotic
Triple Uses
- first aid to help prevent infection in
- minor cuts
- scrapes
- burns
Triple Warnings
For external use only

Allergy alert do not use if you are allergic to any of the ingredients
Do not use
- in the eyes
- over large areas of the body
Ask a doctor before use if you have
- a deep or puncture wounds
- animal bites
- serious burns
Stop use and ask a doctor if
- the condition persists or gets worse
- a rash or other allergic reaction develops
- you need to use longer than 1 week
Keep out of the reach of children

If swallowed, get medical help or contact a Poison Control Center right away.
Triple Directions
- clean the affected area
- apply a small amount of the product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily
- may be covered with a sterile bandage
Triple Other information
- store at 15 0 to 25 0 C (59 0 to 77 0 F)
- tamper evident sealed packets
- do not use if packet is torn or opened
Triple Inactive ingredient

petrolatum
Alcohol Active ingredient

Isopropyl alcohol 70%
Alcohol Purpose

First aid antiseptic
Alcohol Uses
- first aid to help prevent infection in minor cuts, scrapes, and burns
Alcohol Warnings
For external use only

Flammable, keep away from fire or flame.
Do not use
- in the eyes
- over large areas of the body
Ask a doctor before use if you have

deep or puncture wounds

animal bites

serious burns
When using this product
- do not use longer than one week unless directed by a doctor
Stop use and consult a doctor
- if condition persists or gets worse
Keep out of reach of children
- If swallowed, get medical help or contact a Poison Control Center right away.
Alcohol Directions
- clean the affected area
- apply wipe to affected area 1 to 3 times daily
- may be covered with a sterile bandage
- discard wipe after single use
Alcohol Other information

store at room temperature 15 0 to 25 0 C (59 0 to 77 0 F)
Alcohol Inactive ingredient

water
Foille Active ingredient

Benzocaine 5.0% (w/w)

Chloroxylenol 0.1% (w/w)
Foille Purpose

External analgesic

Antiseptic
Foille Uses
- For the temporary relief of pain associated with burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritations.
- First aid to help prevent infection in minor cuts, scrapes and burns.
Foille Warnings
For external use only
When using this product
- avoid contact with the eyes
Stop use and ask a doctor if
- condition worsens, or symptoms persist for more than 7 days or clear up and occur again within a few days.
- Do not apply over large areas of the body. In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor.
Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.
Foille Directions
- clean the affected area.
- adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.
- children under 2 years of age: consult a physician.
Foille Other information

Avoid contact with clothing

Foille may stain certain fabrics
Foille Inactive ingredients

beeswax, benzyl alcohol, calcium disodium EDTA, calcium hydroxide, ceresin, eugenol, hydrogenated vegetable oil, maleic anhydride, mono- and di-glycerides, PEG-32, purified water, sodium borate, sodium lauryl sulfate, zea mays (corn) oil.
Burn Jel Active ingredient

Lidocaine HCl 2.0 %v
Burn Jel Purpose

External analgesic
Burn Jel Uses
- temporarily relieves pain due to minor burns
Burn Jel Warnings
For external use oonly
Do not use
- on large areas of the body, particularly over raw surfaces or blistered areas
When using this product
- avoid contact with eyes
Stop use and ask a doctor if
- the condition gets worse
- symptoms persist for more than 7 days
- condition clears up and recurs within a few days
Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.
Burn Jel Directions
- adults and children 2 years of age and older; apply to affected area not more than 3 to 4 times daily
- children under 2 years of age: ask a doctor
- you may report a serious reaction to this product to 800-430-5490
Burn Jel Other information
- store at room temperature - do not use if opened or torn
Burn Jel Inactive ingredients

carbopol 940, carbopol 1342, diazolidinyl urea, glycerin, melaleuca alternifolia (tea tree) leaf oil, methylparaben, octoxynol-9, propylene glycol, propylparaben, trolamine, water
Burn Jel Questions

1-800-430-5490
Sting Relief Active ingredients (in each wipe)

Ethyl alcohol 50.0%

Lidocaine HCl 2.0%
Sting Relief Purpose

Antiseptic

Topical pain relief
Sting Relief Uses
- prevent infection in minor scrapes, and temporary relief of itching of insect bites
Sting Relief Warnings
For external use only

Flammable, keep away from open fire or flame
Do not use
- over large areas of the body
- in eyes
- over raw or blistered areas
Stop use and ask a doctor

if conditions worsen or persist for more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.
Sting Relief Directions
- adults and children 2 years and older: Apply to cleaned affected area not more than 3 times daily.
- children under 2 years of age: consult a doctor.
Sting Relief Inactive ingredients

benzalkonium chloride, menthol, and purified water
Sting Relief Questions or Comments?

1-800-430-5490
PVP Wipe Active ingredient

Povidone-iodine 10% (equivalent to 1% titratable iodine)
PVP Purpose

First aid antiseptic
PVP USes
- first aid antiseptic to help prevent infection in minor cuts, scrapes and burns
PVP Warnings
For external use only.
Ask a doctor before use if you have
- deep or puncture wounds
- animal bites
- serious burns
Stop use and ask a doctor if
- condition worsens or persists for more than 72 hours
- irritation and redness develops
Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.
PVP Directions
- clean the affected area
- apply1 to 3 times daily
- may be covered with a sterile bandage
- if bandaged, let dry first
- discard wipe after single use
PVP Other information
- do not use on individuals who are allergic or sensitive to iodine
- store at controlled temperature 59-86ºF (15-30ºC)
- do not use if pouch is open or torn
PVP Inactive ingredients

nonoxynol 9, water
PVP Questions

800-430-5490
Aypanal EX Active ingredient

Acetaminophen 500 mg
Aypanal EX Purpose

Pain reliever/fever reducer
Aypanal EX Uses
- temporarily relieves minor aches and pains due to the common cold and headache
- temporarily reduces fever
Aypanal EX Warnings
Liver Warning: This product contains acetaminophen. Severe liver damage may occur if you take:
- more than 4,000 mg in 24 hours, which is the maximum daily amount.
- with other drugs containing acetaminophen
- adult has 3 or more alcoholic drinks every day while using this product
Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:
- skin reddening
- blisters
- rash
If skin reaction occurs, stop use and seek medical help right away
Do Not Use
- with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
Ask a doctor before use if you have
- liver disease
Ask a doctor or pharmacist before use if
- you are taking the blood thinning drug warfarin
Stop use and ask a doctor if
- pain gets worse or lasts more than 10 days
- fever gets worse or lasts more than 3 days
- new symptoms occur
- redness or swelling is present
Keep out of reach of children.

Overdose warning: In case ofl overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.
If pregnant or breastfeeding,
- ask a health professional before use.
Aypanal EX Directions
- do not take more than directed (see overdose warning)
- adults and children 12 years of age and over: Take 2 tablets with water every 6 hours while symptoms last.
- do not take any more than 8 tablets in 24 hours.
- children under 12: consult a doctor
Aypanal EX Other information

store at room temperature 15 0 -30 0 C (59 0 -86 0 F)
TAMPER EVIDENT- DO NOT USE IF OPEN OR TORN
Aypanal EX Inactive ingredients

microcrystalline cellulose, povidone, sodium starch glycolate, starch, stearic acid
Aypanal EX Questions or Comments?

1-800-430-5490
BZK Active ingredient

Benzalkonium chloride 0.13% w/v
BZK Purpose

First aid antiseptic
BZK Uses

Antiseptic cleansing of face, hands, and body without soap and water
BZK Warnings
For external use only
Do not use
- in the eyes or over large areas of the body
- on mucous membranes
- on irritated skin
- in case of deep puncture wounds, animal bites or serious burns, consult a doctor
- longer than 1 week unless directed by a doctor
Stop use and ask a doctor if
- if irritation, redness or other symptoms develop
- the condition persists or gets worse
Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.
BZK Directions
- tear open packet and use as a washcloth
BZK Other information
- store at room temperature 15 0 to 30 0C (59 0 - 86 0 F)
- do not reuse towelette
BZK Inactive ingredients

water
BZK Questions

1-800-430-5490
4334 Z019819 KIT CONTENTS

1 TRIPLE ANTIBIOTIC 10 PER

1 INSTANT COLD PACK 4" X 6"

2 ADHESIVE BDG,PLSTIC,1"X3"16PER

1 BURN JEL 1/8 OZ, 6 PER

1 ALCOHOL PREP PADS 10P

1 PVP IODINE WIPES 10 PER

1 NITRILE GLOVES 2PR BBP

1 ANTIMCRBL ANTSPTC TWLETTS

1 ADHESIVE TAPE W/P 1/2"X 5 YD

1 TWEEZER PLASTICS 4"

1 FLEXICON 2"X 4.1 YD

1 FIRST AID GUIDE ASHI

1 ABD COMBINE PAD 5" X 9"

1 SCISSOR BDGE 4" RED PLS HDL

LBL STOCK 6-3/8"X4"

LBL STOCK 4"X2-7/8"

1 LBL STOCK 3"x1-7/8"

1 LBL CONTS 6 3/4"X3 1/2" ID B

1 LABEL COVER, GRAINGER Z019819

1 KIT PP 24 UNIT FA

3 SAFETEC STING RELIEF WIPES BULK

1 FOILLE BURN/F A OINT 1/2 OZ

4 GAUZE PADS 2"X2" 12PLY

1 GAUZE PADS 4"X4" 12PLY

4 WOVEN FINGERTIP BANDAGE 2"

4 WOVEN KNUCKLE BANDAGE

4 HEAVY FLEX LARGE PATCH 2" X 3"

1 GAUZE PADS 3"X3" 4/BX

1 TRIANG 37X37X52 UNIT

8 AYPANAL EXTRA BULK 2/PK
4379 Z63158002 Kit Contents

1 TRIPLE ANTIBIOTIC 10 PER

1 INSTANT COLD PACK 4" X 6"

2 ADHESIVE BDG,PLSTIC,1"X3"16PER

1 BURN JEL 1/8 OZ, 6 PER

1 ALCOHOL PREP PADS 10P

1 PVP IODINE WIPES 10 PER

1 NITRILE GLOVES 2PR BBP

1 ANTIMCRBL ANTSPTC TWLETTS

1 ADHESIVE TAPE W/P 1/2"X 5 YD

1 TWEEZER PLASTICS 4"

1 FLEXICON 2"X 4.1 YD

1 FIRST AID GUIDE ASHI

1 ABD COMBINE PAD 5" X 9"

1 SCISSOR BDGE 4" RED PLS HDL

LBL STOCK 6-3/8"X4"

LBL STOCK 4"X2-7/8"

1 LBL STOCK 3"x1-7/8"

1 LBL CONTS 6 3/4"X3 1/2" ID B

1 LABEL COVER, GRAINGER Z019819

1 KIT PP 24 UNIT FA

3 SAFETEC STING RELIEF WIPES BULK

1 FOILLE BURN/F A OINT 1/2 OZ

4 GAUZE PADS 2"X2" 12PLY

1 GAUZE PADS 4"X4" 12PLY

4 WOVEN FINGERTIP BANDAGE 2"

4 WOVEN KNUCKLE BANDAGE

4 HEAVY FLEX LARGE PATCH 2" X 3"

1 GAUZE PADS 3"X3" 4/BX

1 TRIANG 37X37X52 UNIT

8 AYPANAL EXTRA BULK 2/PK
Triple Principal Display Panel
Alcohol Principal Display Panel
Foille Principal Display Panel
Burn Jel Principal Display Panel
Sting Relief Principal Display Panel
PVP Principal Display Panel
Aypanal EX Principal Display Panel
BZK Principal Display Panel
4334 Kit Label Z019819
4373 Kit Label Z63158002

INGREDIENTS AND APPEARANCE

4379 FIRST AID KIT
4379 first aid kit kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0498-4379

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-4379-01	1 in 1 KIT; Type 0: Not a Combination Product	10/18/2018

Part #	Package Quantity	Total Product Quantity
Quantity of Parts
Part 1	10 POUCH	4 mL
Part 2	1 TUBE	14 g
Part 3	6 PACKET	21 g
Part 4	1 PACKET	1.4 mL
Part 5	3 POUCH	1.2 mL
Part 6	10 POUCH	3 mL
Part 7	8 PACKET	16
Part 8	10 PACKET	9 g

Part 1 of 8

ALCOHOL WIPE
isopropyl alcohol swab

Product Information
Item Code (Source)	NDC:0498-0143
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mL in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0143-04	0.4 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		09/18/2018

Part 2 of 8

BLISTEX FOILLE MEDICATED FIRST AID
benzocaine and chloroxylenol ointment

Product Information
Item Code (Source)	NDC:10157-9302
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.1 g in 100 g
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	5 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
CERESIN (UNII: Q1LS2UJO3A)
EUGENOL (UNII: 3T8H1794QW)
MALEIC ANHYDRIDE (UNII: V5877ZJZ25)
POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
CORN OIL (UNII: 8470G57WFM)
SODIUM BORATE (UNII: 91MBZ8H3QO)
YELLOW WAX (UNII: 2ZA36H0S2V)
CALCIUM HYDROXIDE (UNII: PF5DZW74VN)
WATER (UNII: 059QF0KO0R)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
BENZYL ALCOHOL (UNII: LKG8494WBH)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1		14 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		03/05/2013

Part 3 of 8

BURN JEL
gel for burns gel

Product Information
Item Code (Source)	NDC:0498-0203
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	2 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
OCTOXYNOL-9 (UNII: 7JPC6Y25QS)
TEA TREE OIL (UNII: VIF565UC2G)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLPARABEN (UNII: A2I8C7HI9T)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0203-00	3.5 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		09/19/2018

Part 4 of 8

ANTISEPTIC TOWELETTE
benzalkonium chloride liquid

Product Information
Item Code (Source)	NDC:0498-0501
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0501-00	1.4 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		12/21/2017

Part 5 of 8

STING RELIEF PAD
ethyl alcohol, lidocaine swab

Product Information
Item Code (Source)	NDC:0498-0733
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	20 mg in 1 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.5 mL in 1 mL

Ingredient Name	Strength
Inactive Ingredients
MENTHOL (UNII: L7T10EIP3A)
WATER (UNII: 059QF0KO0R)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1		0.4 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		12/23/2017

Part 6 of 8

PVP IODINE WIPE
povidone-iodine 10% swab

Product Information
Item Code (Source)	NDC:0498-0121
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	10 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
NONOXYNOL-9 (UNII: 48Q180SH9T)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0121-00	0.3 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		09/18/2018

Part 7 of 8

AYPANAL EX
acetaminophen tablet

Product Information
Item Code (Source)	NDC:0498-2110
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	500 mg

Ingredient Name	Strength
Inactive Ingredients
STEARIC ACID (UNII: 4ELV7Z65AP)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
STARCH, CORN (UNII: O8232NY3SJ)
POVIDONE (UNII: FZ989GH94E)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	12mm
Flavor		Imprint Code	FR1
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-2110-01	2 in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		01/02/2017

Part 8 of 8

TRIPLE ANTIBIOTIC
bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointment

Product Information
Item Code (Source)	NDC:0498-0750
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K)	POLYMYXIN B	5000 [iU] in 1 g
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN	400 [iU] in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN	3.5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
PETROLATUM (UNII: 4T6H12BN9U)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0750-35	0.9 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		09/19/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		10/18/2018

4334 FIRST AID KIT
4334 first aid kit kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0498-4334

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-4334-01	1 in 1 KIT; Type 0: Not a Combination Product	10/18/2018

Part #	Package Quantity	Total Product Quantity
Quantity of Parts
Part 1	1 PACKET	1.4 mL
Part 2	3 POUCH	1.2 mL
Part 3	10 POUCH	3 mL
Part 4	8 PACKET	16
Part 5	10 PACKET	9 g
Part 6	10 POUCH	4 mL
Part 7	1 TUBE	14 g
Part 8	6 PACKET	21 g

Part 1 of 8

ANTISEPTIC TOWELETTE
benzalkonium chloride liquid

Product Information
Item Code (Source)	NDC:0498-0501
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0501-00	1.4 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		12/21/2017

Part 2 of 8

STING RELIEF PAD
ethyl alcohol, lidocaine swab

Product Information
Item Code (Source)	NDC:0498-0733
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	20 mg in 1 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.5 mL in 1 mL

Ingredient Name	Strength
Inactive Ingredients
MENTHOL (UNII: L7T10EIP3A)
WATER (UNII: 059QF0KO0R)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1		0.4 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		12/23/2017

Part 3 of 8

PVP IODINE WIPE
povidone-iodine 10% swab

Product Information
Item Code (Source)	NDC:0498-0121
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	10 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
NONOXYNOL-9 (UNII: 48Q180SH9T)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0121-00	0.3 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		09/18/2018

Part 4 of 8

AYPANAL EX
acetaminophen tablet

Product Information
Item Code (Source)	NDC:0498-2110
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	500 mg

Ingredient Name	Strength
Inactive Ingredients
STEARIC ACID (UNII: 4ELV7Z65AP)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
STARCH, CORN (UNII: O8232NY3SJ)
POVIDONE (UNII: FZ989GH94E)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	12mm
Flavor		Imprint Code	FR1
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-2110-01	2 in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		01/02/2017

Part 5 of 8

TRIPLE ANTIBIOTIC
bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointment

Product Information
Item Code (Source)	NDC:0498-0750
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K)	POLYMYXIN B	5000 [iU] in 1 g
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN	400 [iU] in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN	3.5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
PETROLATUM (UNII: 4T6H12BN9U)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0750-35	0.9 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		09/19/2018

Part 6 of 8

ALCOHOL WIPE
isopropyl alcohol swab

Product Information
Item Code (Source)	NDC:0498-0143
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mL in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0143-04	0.4 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		09/18/2018

Part 7 of 8

BLISTEX FOILLE MEDICATED FIRST AID
benzocaine and chloroxylenol ointment

Product Information
Item Code (Source)	NDC:10157-9302
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.1 g in 100 g
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	5 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
BENZYL ALCOHOL (UNII: LKG8494WBH)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
CERESIN (UNII: Q1LS2UJO3A)
EUGENOL (UNII: 3T8H1794QW)
MALEIC ANHYDRIDE (UNII: V5877ZJZ25)
POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
CORN OIL (UNII: 8470G57WFM)
SODIUM BORATE (UNII: 91MBZ8H3QO)
YELLOW WAX (UNII: 2ZA36H0S2V)
CALCIUM HYDROXIDE (UNII: PF5DZW74VN)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1		14 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		03/05/2013

Part 8 of 8

BURN JEL
gel for burns gel

Product Information
Item Code (Source)	NDC:0498-0203
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	2 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
OCTOXYNOL-9 (UNII: 7JPC6Y25QS)
TEA TREE OIL (UNII: VIF565UC2G)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLPARABEN (UNII: A2I8C7HI9T)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0203-00	3.5 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		09/19/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		10/18/2018

Labeler - Honeywell Safety Products USA, INC (118768815)

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Published Date (What is this?)	Version	Files
Jan 23, 2024	7 (current)	download
Jan 15, 2024	6	download
Dec 30, 2022	5	download
Dec 14, 2021	4	download
Sep 24, 2019	2	download
Jul 29, 2019	1	download

	RxCUI	RxNorm NAME	RxTTY
1	198440	acetaminophen 500 MG Oral Tablet	PSN
2	198440	acetaminophen 500 MG Oral Tablet	SCD
3	198440	APAP 500 MG Oral Tablet	SY
4	199005	benzocaine 5 % / chloroxylenol 0.1 % Topical Ointment	PSN
5	199005	benzocaine 0.05 MG/MG / chloroxylenol 0.001 MG/MG Topical Ointment	SCD
6	199005	benzocaine 5 % / chloroxylenol 0.1 % Topical Ointment	SY
7	204602	bacitracin 400 UNT / neomycin 3.5 MG / polymyxin B 5000 UNT per GM Topical Ointment	PSN
8	204602	bacitracin 0.4 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 5 UNT/MG Topical Ointment	SCD
9	204602	bacitracin 400 UNT / neomycin 3.5 MG (as neomycin sulfate 5 MG) / polymyxin B 5000 UNT per GM Topical Ointment	SY
10	213034	Foille 5 % / 0.1 % Topical Ointment	PSN
11	213034	benzocaine 0.05 MG/MG / chloroxylenol 0.001 MG/MG Topical Ointment [Foille]	SBD
12	213034	Foille (benzocaine 5 % / chloroxylenol 0.1 % ) Topical Ointment	SY
13	797544	isopropyl alcohol 70 % Medicated Pad	PSN
14	797544	isopropyl alcohol 0.7 ML/ML Medicated Pad	SCD
15	797544	isopropyl alcohol 70 % Medicated Pad	SY
16	797544	isopropyl alcohol 70 % Topical Cloth	SY
17	797544	isopropyl alcohol 70 % Topical Swab	SY
18	1011852	lidocaine HCl 2 % Topical Gel	PSN
19	1011852	lidocaine hydrochloride 0.02 MG/MG Topical Gel	SCD
20	1011852	lidocaine hydrochloride 2 % Topical Jelly	SY
21	1038558	benzalkonium chloride 0.13 % Medicated Pad	PSN
22	1038558	benzalkonium chloride 1.3 MG/ML Medicated Pad	SCD
23	1038558	benzalkonium chloride 0.13 GM per 100 GM Topical Pad	SY
24	1038558	benzalkonium chloride 0.13 GM per 100 GM Topical Swab	SY
25	1038558	benzalkonium chloride 0.13 % Topical Swab	SY
26	1038558	benzalkonium chloride 1 ML per 750 ML Topical Swab	SY
27	1190560	ethanol 50 % / lidocaine HCl 2 % Medicated Pad	PSN
28	1190560	ethanol 0.5 ML/ML / lidocaine hydrochloride 20 MG/ML Medicated Pad	SCD
29	1190560	ethanol 50 % / lidocaine hydrochloride 2 % Medicated Pad	SY
30	2056934	Burn Jel 2 % Topical Gel	PSN
31	2056934	lidocaine hydrochloride 0.02 MG/MG Topical Gel [Burn Jel]	SBD
32	2056934	Burn Jel 0.02 MG/MG Topical Gel	SY
33	2056934	Burn Jel 2 % Topical Gel	SY

	NDC
1	0498-0121-00
2	0498-0143-04
3	0498-0203-00
4	0498-0501-00
5	0498-0750-35
6	0498-2110-01
7	0498-4334-01
8	0498-4379-01

Label: 4379 FIRST AID KIT kit4334 FIRST AID KIT kit

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Keep out of reach of children.

If pregnant or breastfeeding,

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4379 FIRST AID KIT kit4334 FIRST AID KIT kit

Number of versions: 6

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4379 FIRST AID KIT kit4334 FIRST AID KIT kit

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Label: 4379 FIRST AID KIT kit
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4379 FIRST AID KIT kit
4334 FIRST AID KIT kit

4379 FIRST AID KIT kit
4334 FIRST AID KIT kit

4379 FIRST AID KIT kit
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4379 FIRST AID KIT kit
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