Label: 4295 FIRST AID KIT- 4295 first aid kit
-
NDC Code(s):
0498-0203-00,
0498-0501-00,
0498-0750-35,
0498-4295-01, view more59898-420-12
- 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)
- Burn Jel Active ingredient
- Burn Jel Purpose
- Burn Jel Uses
- Burn Jel Warnings
- Burn JEl Directions
- Burn Jel Other information
- Burn Jel Inactive ingredients
- Burn Jel Questions
- Triple Active ingredient
- Triple Purpose
- Triple Uses
-
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
- Triple Directions
- Triple Other information
- Triple Inactive ingredient
- Triple Questions?
- BZK Wipe Active ingredient
- BZK Wipe Purpose
- BzK Wipe Uses
-
BZK Wipe
Warnings
For external use onlyDo 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 Wipe Directions
- BZK Wipe Other information
- BZK Wipe Inactive ingredient
- BZK Wipe Questions
- Hand Sanitizer Active ingredient
- Hand Sanitizer Purpose
- Hand Sanitizer Uses
- Hand Sanitizer Warnings
- Hand Sanitizer Directions
- Hand Sanitizer Other information
- Hand Sanitizer Inactive ingredients
- Hand Sanitizer Questions or Comments?
-
4252
68P2CCU Kit Contents
1 TRIPLE ANTIBIOTIC 10 PER
1 INSTANT COLD PACK 4" X 6"
1 BURN JEL 1/8 OZ, 6 PER
1 POR. CLOTH TAPE 2X10Yd
1 pOR. CLOTH TAPE 1/2X10Y
3 GAUZE CLEAN-WRAP BDGE N/S 4"
1 ABD COMBINE PAD 5" X 9"
1 ABD PADS 8"X10" STERILE
1 ELASTIC BANDAGE 3" X 4.5YD
1 CPR FILTERSHIELD 77-100
1 ANTISEPTIC WIPES BZK CHL 20'S
1 SCISSOR UTILITY SHEARS 7-1/4"
LBL STOCK 6-3/8"X4"
LBL STOCK 4"X2-7/8"
1 LBL STOCK 3"x1-7/8"
3 PR LRG NITRILE GLVES ZIP BAG
1 ANTISEPTIC HAND GEL 4OZ
1 WATER-JEL BURN DRESSING 4 X 4
1 KIT PP 24 UNIT FA
2 TRI BNDG NON WOVEN 40"X40"X56"
1 EYE PADS STD OVAL STERILE
1 GAUZE PADS 4"X4" 12PLY
5 WOVEN FINGERTIP BANDAGE 3"
10 HEAVY FLEX BANDAGE 7/8" X 3"
5 HEAVY FLEX KNUCKLE BANDAGE
5 HEAVY FLEX LARGE PATCH 2" X 3"
1 ZIP-LOCK BAG 5" X 5" .002
- Burn Jel Principal Display Panel
- Triple Principal Display Panel
- BZK Wipe Principal Display Panel
- Hand Sanitizer Principal Display Panel
- 4295 Kit Label SF00002877
-
INGREDIENTS AND APPEARANCE
4295 FIRST AID KIT
4295 first aid kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4295 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4295-01 1 in 1 KIT 09/13/2018 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 6 PACKET 21 g Part 2 10 PACKET 9 g Part 3 1 PACKET 1.4 mL Part 4 1 BOTTLE, PLASTIC 118 mL Part 1 of 4 BURN JEL
gel for burns gelProduct Information Item Code (Source) NDC:0498-0203 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 2 g in 100 g Inactive Ingredients Ingredient Name Strength 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0203-00 3.5 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 09/19/2018 Part 2 of 4 TRIPLE ANTIBIOTIC
bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointmentProduct Information Item Code (Source) NDC:0498-0750 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength 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 Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0750-35 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 09/19/2018 Part 3 of 4 ANTISEPTIC TOWELETTE
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 4 of 4 INSTANT HAND SANITIZER
alcohol liquidProduct Information Item Code (Source) NDC:59898-420 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) TRIISOPROPANOLAMINE (UNII: W9EN9DLM98) CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59898-420-12 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/15/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/13/2018 Labeler - Honeywell Safety Products USA, Inc. (118768815)