Label: 4395 FIRST AID KIT kit
-
NDC Code(s):
0498-0114-01,
0498-0143-04,
0498-0501-00,
0498-0730-01, view more0498-2110-01, 0498-4395-01, 0498-7502-01
- 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.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Alcohol Wipe Active ingredient
- Alcohol Wipe Purpose
- Alcohol Wipe Uses
- Alcohol Wipe Warnings
- Alcohol Wipe Directions
- Alcohol Wipe Other information
- Alcohol Wipe Inactive ingredient
- Alcohol Wipe Questions
- Aspirin Active ingredient (in each tablet)
- Aspirin Purpose
- Aspirin Uses
-
Aspirin
Warnings
Reye's syndrome: Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness.
Allergy alert: Aspirin may cause a severe allergic reaction which may include:
- hives
- facial swelling
- asthma (wheezing)
- shock
Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you:are:
- age 60 or older
- have had stomach ulcers or bleeding problems
- take a blood thinning (anticoagulant) or steroid drug
- take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others)
- have 3 or more alcoholic drinks every day while using this product
- take more or for a longer time than directed
Ask a doctor before use if
- stomach bleeding warning applies to you
- you have a history of stomach problems such as heartburn
- you have high blood pressure, heart disease, liver cirrhosis or kidney disease
- you are taking a diuretic
- you have asthma
Ask a doctor or pharmacist before use if you are
- taking a prescription drug for diabetes, gout or arthritis
Stop use and ask a doctor if
- you experience any of the following signs of stomach bleeding:
- feel faint
- vomit blood
- have bloody or black stools
- have stomach pain that does not get better
- pain gets worse or lasts more than 10 days
- fever gets worse or lasts more than 3 days
- redness or swelling is present in the painful area
- ringing in the ears or loss of hearing occurs
- any new symptoms appear
If pregnant or breast-feeding,
If pregnant or breat-feeding, ask a health professional before use. It is especially important not to use aspirin during the last three months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.
- Aspirin Directions
- Aspirin Other information
- Aspirin Inactive ingredients
- Aspirin Questions or Comments
- BZK Active ingredient
- BZK Purpose
- BZK Uses
-
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
- BZK Directions
- BZK Other information
- BZK Inactive ingredient
- BZK Questions
- Neomycin Active ingredient (each gram contains)
- Neomycin Purpose
- Neomycin Uses
- Neomycin Warnings
- Neomycin Directions
- Neomycin Other information
- Neomycin Inactive ingredient
- Neomycin Questions
- Aypanal EX Active ingredient
- Aypanal EX Purpose
- Aypanal EX Uses
-
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.
- Aypanal EX Directions
- Aypanal EX Other information
- Aypanal EX Inactive ingredients
- Aypanal EX Questions or Comments?
- FABC Active ingredient
- FABC Purpose
- FABC Uses
-
FABC
Warnings
For external use only
Do not use
- in or near the eyes
- if you are allergic to any of the ingredients
- lin large areas of the body, particularly over raw surfaces or blistered areas
- for more than 10 days
- FABC Direcctions
- FABC Other information
- FABC Inactive ingredients
- FABC Questions
- Cedaprin Active ingredient
- Cedaprin Purpose
- Cedaprin Uses
-
Cedaprin
Warnings
Allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:
- hives
- facial swelling
- asthma (wheezing)
- shock
- skin reddening
- rash
- blisters
If an allergic reaction occurs, stop use and seek medical help right away.
Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you
- are age 60 or older
- have had stomach ulcers or bleeding problems
- take a blood thinning (anticoagulant) or steroid drug
- take other drugs containing prescription or nonprescription NSAIDs [aspirin, ibuprofen, naproxen, or others]
- have 3 or more alcoholic drinks every day while using this product
- take more or for a longer time than directed
Heart attack and stroke warning:
- NSAID's, except aspirin, increase the risk of heart attack, heart failure, and stroke. These can be fatal. The risk is higher if you use more than directed or for longer than directed.
Do not use
- if you have ever had an allergic reaction to ibuprofen or any other pain reliever/fever reducer
- right before or after heart surgery
Ask a doctor before use if
- you have problems or serious side effectsfrom taking pain relievers or fever reducers
- stomach bleeding warning applies to you
- you have a history of stomach problems such as heartburn
- you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma or had a stroke
- you are taking a diuretic
Ask a doctor or a pharmacist before use if you are
- taking aspirin for heart attack or stroke, because ibuprofen may decrease the benefit of aspirin
- under a doctors care for any serious condition
- taking any other drug
Stop use and ask a doctor if
- you experience any of the following signs of stomach bleeding:
- feel faint
- vomit blood
- have bloody or black stools
- have stomach pain that does not get better
- you have symptoms of heart problems or stroke:
- chest pain
- trouble breathing
- weakness in oe part or side of body
- slurred speech
- leg swelling
- pain gets worse or lasts more than 10 days
- fever gets worse or lasts more than 3 days
- redness or swelling is present in the painful area
- any new symptoms appear
-
Cedaprin
Directions
- do not take more than directed
- the smallest effective dose should be used
- adult and children 12 years of age and over:
- take 1 tablet every 4 to 6 hours while symptoms persist
- if pain or fever does not respond to 1 tablet, 2 tablets may be used
- do not exceed 6 tablets in 24 hours, unless directed by a doctor
- children under 12 years: ask a doctor
- Cedaprin Other information
- Cedaprin Inactive ingredients
- Cedaprin Questions or Comments?
-
4395
Z019840 KIT CONTENTS
1 XTRA LRG 2" X 4" AWC
1 ADHESIVE TAPE W/P 1/2"X 5 YD
1 TWEEZER PLASTICS 4"
1 FIRST AID GUIDE ASHI
1 EMERGENCY SURVIVAL BLANKET
1 ABD COMBINE PAD 5" X 9"
10 CTA 3" SINGLE TIP
1 TONGUE BLADES SR WRAPPED
LBL STOCK 6-3/8"X4"
LBL STOCK 4"X2-7/8"
1 LBL STOCK 3"x1-7/8"
1 LBL CONTS 8"X8",CUSTOM ID B
12 BZK ANTISEPTIC WIPE, BULK
1 SOFT PACK, CLOTH BAG- MEDIUM
1 PR LRG NITRILE GLVES ZIP BAG
1 FIRST AID CREAM 1.0GR PKT EACH
1 SWIFT 3/4" X 3" PLAS 50 ZIPBAG
4 POUCH NEOMYCIN ANTIBIOTIC .9 G
5 ADH BANDAGE BUTTERFLY 1980000
8 WIPE ALCOHOL PREP IPA 70% (DUKAL)
20 ADH BANDAGE 3/8" X 1 1/2" DNX
1 COLD PACK UNIT 4"X6" BULK
5 GAUZE PADS 2"X2" 12PLY
1 EYE PADS STD OVAL STERILE
1 GAUZE PADS 3"X3" 12PLY
12 PLASTIC SPOT 7/8" DIAM DNX
20 PLASTIC BANDAGE 1" X 3"
8 WOVEN FINGERTIP BANDAGE 2"
8 WOVEN KNUCKLE BANDAGE
10 WOVEN BANDAGE 1" X 3"
1 ZIP LOCK 2 X 4" 2ML
1 ASPIRIN BULK 2/PK
2 AYPANAL EXTRA BULK 2/PK
1 CEDAPRIN BULK 2/PK
- Alcohol Wipe Label
- Aspirin Principal Display Panel
- BZK Principal Display Panel
- Neomycin Principal Display Panel
- Aypanal EX Principal Display Panel
- FABC Principal Display Panel
- Cedaprin Principal Display Panel
- 4395 Kit Label Z019840
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INGREDIENTS AND APPEARANCE
4395 FIRST AID KITÂ
4395 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4395 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4395-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 8 POUCH 3.2 mL Part 2 1 PACKET 2 Part 3 4 PACKET 3.6 g Part 4 12 PACKET 16.8 mL Part 5 2 PACKET 4 Part 6 1 PACKET 0.9 g Part 7 1 PACKET 2 Part 1 of 7 ALCOHOL WIPEÂ
isopropyl alcohol swabProduct Information Item Code (Source) NDC:0498-0143 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 0.7 mL  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0143-04 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/18/2018 Part 2 of 7 ASPIRINÂ
aspirin tabletProduct Information Item Code (Source) NDC:0498-0114 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN 325 mg Inactive Ingredients Ingredient Name Strength CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  STEARIC ACID (UNII: 4ELV7Z65AP)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  HYPROMELLOSE 2208 (100 MPA.S) (UNII: B1QE5P712K)  MINERAL OIL (UNII: T5L8T28FGP)  TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code FR21 Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0114-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/18/2018 Part 3 of 7 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 4 of 7 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0501-00 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/22/2017 Part 5 of 7 AYPANAL EXÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2110 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ)  SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  STEARIC ACID (UNII: 4ELV7Z65AP)  POVIDONE (UNII: FZ989GH94E)  MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  Product Characteristics Color white Score no score Shape ROUND Size 12mm Flavor Imprint Code FR1 Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2110-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/02/2017 Part 6 of 7 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  CETYL ALCOHOL (UNII: 936JST6JCN)  PEG-100 STEARATE (UNII: YD01N1999R)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 7 of 7 CEDAPRINÂ
ibuprofen tabletProduct Information Item Code (Source) NDC:0498-7502 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN 200 mg Inactive Ingredients Ingredient Name Strength HYPROMELLOSES (UNII: 3NXW29V3WO)  TRIACETIN (UNII: XHX3C3X673)  POVIDONE K30 (UNII: U725QWY32X)  SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  FERRIC OXIDE RED (UNII: 1K09F3G675)  TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  STARCH, CORN (UNII: O8232NY3SJ)  LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  STEARIC ACID (UNII: 4ELV7Z65AP)  Product Characteristics Color red Score no score Shape ROUND Size 10mm Flavor Imprint Code G;2 Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-7502-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA079129 01/02/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 Labeler - Honeywell Safety Products USA, INC (118768815)