Label: ADVENTURE MEDICAL KITS 1 PERSON FIRST AID- benzalkonium chloride, benzocaine, sd alcohol kit
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Contains inactivated NDC Code(s)
NDC Code(s): 44224-1000-1, 52124-0001-1, 52124-0008-1 - Packager: Tender Corp dba Adventure Medical Kits
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated October 25, 2010
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- DO NOT USE
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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PRINCIPAL DISPLAY PANEL
SURVIVAL TOOLS
1 Slim Rescue Howler Whistle
6 antiseptic wound wipe
1 sting relief wipe
10 Bandage, adhesive, fabric 1" x 3"
2 Bandage, Adhesive, Fabric, Knuckle
1 Bandage Adhesive, Extra Large
2 Bandage, Butterfly Closure
4 Dressing, Gauze, Sterile 2"x2"
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- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ADVENTURE MEDICAL KITS 1 PERSON FIRST AID
benzalkonium chloride, benzocaine, sd alcohol kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44224-1000 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:44224-1000-1 1 in 1 KIT Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 6 PACKAGE 4.8 mL Part 2 1 PACKAGE 0.5 mL Part 1 of 2 ANTISEPTIC TOWELETTE
benzalkonium chloride swabProduct Information Item Code (Source) NDC:52124-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.4 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52124-0001-1 0.8 mL in 1 PACKAGE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 08/25/2010 Part 2 of 2 INSECT STING RELIEF PAD
benzocaine,alcohol swabProduct Information Item Code (Source) NDC:52124-0008 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 6 mL in 100 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 60 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52124-0008-1 0.5 mL in 1 PACKAGE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part348 08/25/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part348 08/25/2010 Labeler - Tender Corp dba Adventure Medical Kits (064437304) Registrant - GFA Production (Xiamen) Co., Ltd. (421256261) Establishment Name Address ID/FEI Business Operations GFA Production (Xiamen) Co., Ltd 421256261 manufacture