Label: ADVENTURE FIRST AID WATER RESISTANT- benzocaine, alcohol kit
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Contains inactivated NDC Code(s)
NDC Code(s): 44224-0120-1, 52124-0001-1, 52124-0008-1, 52124-0017-1 - Packager: Tender Corporation
- Category: HUMAN OTC DRUG LABEL
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 March 15, 2017
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient - Antiseptic
- Purpose - Antiseptic
- Use - Antiseptic
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Warnings, Precautions and Directions - Antiseptic
For External use only.
Keep out of Reach of Children.
Stop use if unusual redness, swelling or other symptoms occur, consult a physician immediately.
Do not uses in eyes or over large areas of the body.
Tear open packet, unfold towelette and use to cleanse desired skin area. Discard towelette appropriately after single use.
- Inactive Ingredients - Antiseptic
- Active Ingredient - Alcohol Prep Pad
- Use - Alcohol Prep Pad
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Warnings, Precautions and Directions - Alcohol Prep Pad
For External Use Only
Flammable - Keep away from fire or flame
Do Not Use - with electrocautery, in eyes
Stop Use and Ask a Doctor if - Irritation or redness develop and persists for more than 72 hours
Keep out of Reach of Children
If swallowed, get medical help or contact a poison control center right away.
Tear Open packet, unfold and use as and wipe injection site vigorously and discard.
Store at Room Temperature
- Active Ingredients - Insect Relief Pad
- Purpose - Insect Relief Pad
- Use - Insect Relief Pad
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Warnings, Precautions and Directions - Insect Relief Pad
Clean intended area thoroughly with pad. Discard after single use
Warnings: For external use only.
Avoid contact with eyes. If this happens, rinse thoroughly with water
If swallowed, get medical help or contact a Poison Control Center right away
Flammable - keep away from fire or flame
Do not use: In eyes, on broken skin, deep puncture wounds. If unusual redness, swelling, irritation or other symptoms occur, consult a physician immediately.
- Adventure First Aid Water Resistant
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INGREDIENTS AND APPEARANCE
ADVENTURE FIRST AID WATER RESISTANT
benzocaine, alcohol kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44224-0120 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:44224-0120-1 1 in 1 BOX; Type 0: Not a Combination Product 10/01/2015 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 4 PACKAGE 3 mL in .8 Part 2 2 PACKAGE 1 mL in .5 Part 3 4 PACKAGE 3 mL in .7 Part 1 of 3 ANTISEPTIC
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 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:52124-0001-1 0.8 mL in 1 PACKAGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/23/2010 Part 2 of 3 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 0.6 mg 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; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 04/23/2011 Part 3 of 3 ALCOHOL PREP PAD
isopropyl alcohol swabProduct Information Item Code (Source) NDC:52124-0017 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 700 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:52124-0017-1 0.7 mL in 1 PACKAGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 02/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 10/01/2015 Labeler - Tender Corporation (064437304) Registrant - Tender Corporation (064437304) Establishment Name Address ID/FEI Business Operations Tender Corporation 064437304 manufacture(44224-0120)
