DailyMed - 4293 FIRST AID KIT- 4293 first aid kit

NDC Code(s): 0498-0100-01, 0498-0121-00, 0498-0143-04, 0498-0203-00, view more
0498-0733-00, 0498-0750-35, 0498-0800-34, 0498-3334-00, 0498-4293-01
Packager: Honeywell Safety Products USA, Inc.

Category: HUMAN OTC DRUG LABEL
DEA Schedule: None
Marketing Status: unapproved drug other

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 October 16, 2019

If you are a consumer or patient please visit this version.

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Burn Jel Active ingredient

Lidocaine HCl 2.0%
Burn Jel Purpose

External analgesic
Burn Jel Uses
- temporarily relieves pain due to minor burns
Burn Jel Warnings
For external use only
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
Triple Active ingredient

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
Triple Questions?

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

Ethyl alcohol 50.0%

Lidocaine HCl 2.0%
Sting Relief Purposse

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
Eyewash Active ingredient

Sterile Water 99%
Eyewassh Purpose

Eyewash
Eyewash Uses
- for flushing the eye to remove loose foreign material, air pollutants or chlorinated water
Eyewash Warnings
For external use only
- Obtain immediate medical treatment for all open wounds in or near eyes.
- To avoid contamination, do not touch tip of container to any surface.
- Do not reuse.
- Once opened, discard.
Do not use
- if solution changes color or becomes cloudy
- if you have open wounds in or near the eyes, get medical help right away.
Stop use and ask a doctor if
- you experience eye pain
- changes in vision
- continued redness or irritation of the eye
- condition worsens or persists
Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.
Eyeash Directions
- remove contacts before using
- twist top to remove
- flush the affected area as needed
- control rate of flow by pressure on the bottle
- if necessary, continue flushing with emergency eyewash or shower
Eyewash Inactive ingredients

sodium chloride, sodium phosphate dibasic, sodium phosphate monobasic
Eyeash Questions

Call 1-800-430-5490 Honeywell Safety Products USA, Inc. Smithfield, RI 02917
Hydrocortisone Active ingredient (in each gram)

Hydrocortisone acetate (equivalent to Hydrocortisone 1%)
Hydrcortisone Purpose

Anti-itch cream
Hydrocortisone Uses
- for the temporary relief of itching associated with minor skin irritations and rashes
Hydrocortisone Warnings
For external use only
Ask a doctor before use if
- you are using any other hydrocortisone product
When using the product
- avoid contact with eyes
- do not begin use of any other hydrocortisone product unless you have consulted a doctor
- do not use for the treatment of diaper rash
Stop use and ask a doctor if
- condition worsens
- condition persists 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.
Hydrocortisone Directions
- adults and children 2 years and older:
- clean the affected area
- apply to the area not more than 3 to 4 times daily
- children under 2 years of age: consult a doctor
Hydrocortisone Other information
- store at room temperature (do not freeze)
Hydrocortisone Inactive ingredients

cetyl alcohol, citric acid, diazolidinyl urea, edetate disodium, glycerin, glyceryl monostearate, methylparaben, mineral oil, polyethylene glycol, propylene glycol, propylparaben, purified water, stearic acid, trolamine
Hydrocortisone Questions or Comments?

1-800-430-5490
Ammonia Active ingredient

Ammonia 15%
Ammonia Purpose

Respiratory stimulant
Ammonia Uses
- to prevent or treat fainting
Ammonia Warnings
For external use only
Do not use
- if you have breathing problems such as asthma or emphysema
Stop use and ask a doctor if
- condition persists
Keep out of reach of children

If swallowed get medical help or contact a Poison Control Center right away.
Ammonia Directions

hold inhalant away from face and crush ampoule between thumb and forefinger at position indicated on sleeve.

hold near nostrils for inhalation of volatile vapor
Ammonia Other information
- store at room temperature away from light
Ammonia Inactive ingredients

alcohol USP, FD&C red #40, lavender oil, lemon oil fcc, nutmeg oil, purified water
Ammonia Questions or Comments?

1-800-430-5490
Alcohol Active ingredient

Isopropyl alcohol 70%
Alcohol Purpose

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

Flammable, keep away from fire and flame
Do not use
- in or near 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 1 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
- may be covered with a sterile bandage
- apply wipe to affeted are 1 to 3 times daily
- discard wipe after single use
Alcohol Other information
- store at room temperature 15 0 to 25 0 C (59 0 to 77 0 F)
- do not use if packet is torn or opened
Alcohol Inactive ingredient

water
Alcohol Questions

1-800-430-5490
PVP 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
4293 SF00004080 Kit Contents

1 FNGRTIP-5 PER, KNCKL BDG-4 PER

1 TRIPLE ANTIBIOTIC 10 PER

1 AMMONIA INHALANTS 10 PER

1 EYE DRESS PKT W/4 ADH STRIPS

1 TRIANGULAR BDG, NON-STERILE

1 FORCEPS & SCISSORS, 1 EA

1 GAUZE BANDAGE, 2" X 6 YD,2 PER

1 INSTANT COLD PACK 4" X 6"

1 ADH BDG W/NOADHR PAD,1X3 32PER

1 BURN JEL 1/8 OZ, 6 PER

1 ALCOHOL PREP PADS 10P

1 HYDROCORTISON,1.O%,1/32 OZ,10P

1 PVP IODINE WIPES 10 PER

1 STING RELIEF WIPES 10 PER BOX

1 ADH TAPE W/P 1/2"X 2 1/2 YD

1 FIRST AID GUIDE ASHI

1 1 OZ, BUFF EYEWASH

1 BANDAGE COMP 4" W/TELFA PAD 1

LBL STOCK 6-3/8"X4"

LBL STOCK 4"X2-7/8"

1 LBL STOCK 3"x1-7/8"

1 KIT STL 24 UN WHITE 01
Burn Jel Principal Display Panel
Triple Principal Display Panel
Sting Relief Principal Display Panel
Eyewash Principal Display Panel
Hydrocortisone Principal Display Panel
Ammonia Principal Display Panel
Alcohol Principal Display Panel
PVP Principal Display Panel
4293 Kit Label SF-00004080

INGREDIENTS AND APPEARANCE

4293 FIRST AID KIT
4293 first aid kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0498-4293

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-4293-01	1 in 1 KIT	09/13/2018

Part #	Package Quantity	Total Product Quantity
Quantity of Parts
Part 1	6 PACKET	21 g
Part 2	1 BOTTLE	30 mL
Part 3	10 PACKET	9 g
Part 4	10 POUCH	4 mL
Part 5	10 POUCH	4 mL
Part 6	10 PACKET	9 g
Part 7	10 AMPULE	3 mL
Part 8	10 POUCH	3 mL
Part 9	10 PACKET	9 g

Part 1 of 9

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
TEA TREE OIL (UNII: VIF565UC2G)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
METHYLPARABEN (UNII: A2I8C7HI9T)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERIN (UNII: PDC6A3C0OX)
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)
DIPROPYLENE GLYCOL (UNII: E107L85C40)

#	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
OTC monograph not final	part348	09/19/2018

Part 2 of 9

EYESALINE EMERGENCY EYEWASH
purified water liquid

Product Information
Item Code (Source)	NDC:0498-0100
Route of Administration	OPHTHALMIC

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R)	WATER	98.6 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0100-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part349	12/18/2018

Part 3 of 9

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
OTC monograph final	part333B	09/19/2018

Part 4 of 9

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
OTC monograph not final	part333A	09/18/2018

Part 5 of 9

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
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
MENTHOL (UNII: L7T10EIP3A)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0733-00	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
OTC monograph not final	part348	12/23/2017

Part 6 of 9

HYDROCORTISONE
anti-itch cream ointment

Product Information
Item Code (Source)	NDC:0498-0800
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HYDROCORTISONE ACETATE (UNII: 3X7931PO74) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE ACETATE	1 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
LIGHT MINERAL OIL (UNII: N6K5787QVP)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
CETYL ALCOHOL (UNII: 936JST6JCN)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
EDETATE DISODIUM (UNII: 7FLD91C86K)
STEARIC ACID (UNII: 4ELV7Z65AP)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
TROLAMINE (UNII: 9O3K93S3TK)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0800-34	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
OTC monograph not final	part348	03/06/2013	10/15/2019

Part 7 of 9

AMMONIA INHALENT
ammonia inhalent inhalant

Product Information
Item Code (Source)	NDC:0498-3334
Route of Administration	RESPIRATORY (INHALATION)

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X)	AMMONIA	0.045 g in 0.3 mL

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-3334-00	0.3 mL in 1 AMPULE; 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 8 of 9

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
WATER (UNII: 059QF0KO0R)
NONOXYNOL-9 (UNII: 48Q180SH9T)

#	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 9 of 9

HYDROCORTISONE
anti-itch cream

Product Information
Item Code (Source)	NDC:0498-0801
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HYDROCORTISONE ACETATE (UNII: 3X7931PO74) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE ACETATE	1 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
LIGHT MINERAL OIL (UNII: N6K5787QVP)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
CETYL ALCOHOL (UNII: 936JST6JCN)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
EDETATE DISODIUM (UNII: 7FLD91C86K)
STEARIC ACID (UNII: 4ELV7Z65AP)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
TROLAMINE (UNII: 9O3K93S3TK)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1		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
OTC monograph not final	part348	10/15/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		09/13/2018

Labeler - Honeywell Safety Products USA, Inc. (079287321)

Registrant - Honeywell Safety Products USA, Inc. (079287321)

Name	Address	ID/FEI	Business Operations
Establishment
James Alexander		040756421	manufacture(0498-3334)

Name	Address	ID/FEI	Business Operations
Establishment
Honeywell Safety Products USA, Inc		079287321	pack(0498-4293)

Name	Address	ID/FEI	Business Operations
Establishment
Water-Jel Technologies		155522589	manufacture(0498-0203, 0498-0750, 0498-0800, 0498-0801)

Name	Address	ID/FEI	Business Operations
Establishment
Honeywell Safety Products USA, Inc.		167518617	manufacture(0498-0100)

Name	Address	ID/FEI	Business Operations
Establishment
Changzhou Maokang Medical		421317073	manufacture(0498-0143)

Name	Address	ID/FEI	Business Operations
Establishment
Sion Medical Biotext		532775194	manufacture(0498-0121)

Name	Address	ID/FEI	Business Operations
Establishment
Safetec of America Inc		874965262	manufacture(0498-0733)

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Published Date (What is this?)	Version	Files
Oct 17, 2019	2 (current)	download
Apr 29, 2019	1	download

	RxCUI	RxNorm NAME	RxTTY
1	204602	bacitracin 400 UNT / neomycin 3.5 MG / polymyxin B 5000 UNT per GM Topical Ointment	PSN
2	204602	bacitracin 0.4 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 5 UNT/MG Topical Ointment	SCD
3	204602	bacitracin 400 UNT / neomycin 3.5 MG (as neomycin sulfate 5 MG) / polymyxin B 5000 UNT per GM Topical Ointment	SY
4	797544	isopropyl alcohol 70 % Medicated Pad	PSN
5	797544	isopropyl alcohol 0.7 ML/ML Medicated Pad	SCD
6	797544	isopropyl alcohol 70 % Medicated Pad	SY
7	797544	isopropyl alcohol 70 % Topical Cloth	SY
8	797544	isopropyl alcohol 70 % Topical Swab	SY
9	1011852	lidocaine HCl 2 % Topical Gel	PSN
10	1011852	lidocaine hydrochloride 0.02 MG/MG Topical Gel	SCD
11	1011852	lidocaine hydrochloride 2 % Topical Jelly	SY
12	1043690	hydrocortisone acetate 1 % Topical Cream	PSN
13	1043690	hydrocortisone acetate 10 MG/ML Topical Cream	SCD
14	1043690	hydrocortisone acetate 1 % Topical Cream	SY
15	1053173	water 98.6 % Ophthalmic Irrigation Solution	PSN
16	1053173	water 986 MG/ML Ophthalmic Irrigation Solution	SCD
17	1053173	water 98.577 % Ophthalmic Irrigation Solution	SY
18	1053173	water 98.6 ML per 100 ML Ophthalmic Irrigation Solution	SY
19	1053173	water 98.6 % Ophthalmic Irrigation Solution	SY
20	1190560	ethanol 50 % / lidocaine HCl 2 % Medicated Pad	PSN
21	1190560	ethanol 0.5 ML/ML / lidocaine hydrochloride 20 MG/ML Medicated Pad	SCD
22	1190560	ethanol 50 % / lidocaine hydrochloride 2 % Medicated Pad	SY
23	1299889	ammonia 15 % Nasal Inhalant	PSN
24	1299889	ammonia 150 MG/ML Nasal Inhalant	SCD
25	1299889	ammonia 0.045 GM per 0.3 ML Nasal Inhalant	SY
26	1299889	ammonia 0.3 ML Nasal Inhalant	SY
27	1299889	ammonia 15 % Nasal Inhalant	SY
28	1440184	hydrocortisone acetate 1 % Topical Ointment	PSN
29	1440184	hydrocortisone acetate 0.01 MG/MG Topical Ointment	SCD
30	1440184	hydrocortisone acetate 1 % Topical Ointment	SY
31	2056934	Burn Jel 2 % Topical Gel	PSN
32	2056934	lidocaine hydrochloride 0.02 MG/MG Topical Gel [Burn Jel]	SBD
33	2056934	Burn Jel 0.02 MG/MG Topical Gel	SY
34	2056934	Burn Jel 2 % Topical Gel	SY

Label: 4293 FIRST AID KIT- 4293 first aid kit

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Do not use

When using this product

Stop use and ask a doctor if

Keep out of reach of children

Do not use

Stop use and ask a doctor if

Keep out of the reach of children

Do not use

Stop use and ask a doctor

Keep out of reach of children.

Do not use

Stop use and ask a doctor if

Keep out of reach of children

Ask a doctor before use if

When using the product

Stop use and ask a doctor if

Keep out of reach of children

Do not use

Stop use and ask a doctor if

Keep out of reach of children

Do not use

Ask a doctor before use if you have

When using this product

Stop use and consult a doctor if

Keep out of reach of children

Ask a doctor before use if you have

Stop use and ask a doctor if

Keep out of reach of children.

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	NDC
1	0498-0100-01
2	0498-0121-00
3	0498-0143-04
4	0498-0203-00
5	0498-0733-00
6	0498-0750-35
7	0498-0800-34
8	0498-3334-00
9	0498-4293-01

Label: 4293 FIRST AID KIT- 4293 first aid kit

View Package Photos

VIEW MORE

Drug Label Info

Safety

Related Resources

More Info For This Drug

Drug Label Information

Do not use

When using this product

Stop use and ask a doctor if

Keep out of reach of children

Do not use

Stop use and ask a doctor if

Keep out of the reach of children

Do not use

Stop use and ask a doctor

Keep out of reach of children.

Do not use

Stop use and ask a doctor if

Keep out of reach of children

Ask a doctor before use if

When using the product

Stop use and ask a doctor if

Keep out of reach of children

Do not use

Stop use and ask a doctor if

Keep out of reach of children

Do not use

Ask a doctor before use if you have

When using this product

Stop use and consult a doctor if

Keep out of reach of children

Ask a doctor before use if you have

Stop use and ask a doctor if

Keep out of reach of children.

Find additional resources

Safety

Related Resources

More Info on this Drug

4293 FIRST AID KIT- 4293 first aid kit

Number of versions: 2

4293 FIRST AID KIT- 4293 first aid kit

4293 FIRST AID KIT- 4293 first aid kit

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4293 FIRST AID KIT- 4293 first aid kit

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