ADVENTURE FIRST AID WATER RESISTANT- benzocaine, alcohol 
Tender Corporation

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.

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Adventure First Aid Water Resistant

Active Ingredient - Antiseptic

Benzalkonium Chloride 0.13%

Purpose - Antiseptic

Antiseptic

Use - Antiseptic

For Professional and hospital use. Helps prevent infection. Antiseptic cleansing of face, hands and body without soap and water.

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

Purified Water

Active Ingredient - Alcohol Prep Pad

Isopropyl Alcohol 70%

Use - Alcohol Prep Pad

For preparation of the skin before injection

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

Benzocaine 6%

SD alcohol 60%

Purpose - Insect Relief Pad

Topical Anesthetic - Antiseptic

Use - Insect Relief Pad

For the temporary relief of pain and itching associated with minor burns, scrapes and insect bites

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

HangtagHangtagAlcohol PadISRPAntiseptic Wipe

ADVENTURE FIRST AID WATER RESISTANT 
benzocaine, alcohol kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44224-0120
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:44224-0120-11 in 1 BOX; Type 0: Not a Combination Product10/01/2015
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 14 PACKAGE 3 mL  in .8 
Part 22 PACKAGE 1 mL  in .5 
Part 34 PACKAGE 3 mL  in .7 
Part 1 of 3
ANTISEPTIC 
benzalkonium chloride swab
Product Information
Item Code (Source)NDC:52124-0001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52124-0001-10.8 mL in 1 PACKAGE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/23/2010
Part 2 of 3
INSECT STING RELIEF PAD 
benzocaine,alcohol swab
Product Information
Item Code (Source)NDC:52124-0008
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE0.6 mg  in 100 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL60 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52124-0008-10.5 mL in 1 PACKAGE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34804/23/2011
Part 3 of 3
ALCOHOL PREP PAD 
isopropyl alcohol swab
Product Information
Item Code (Source)NDC:52124-0017
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL700 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52124-0017-10.7 mL in 1 PACKAGE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A02/01/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A10/01/2015
Labeler - Tender Corporation (064437304)
Registrant - Tender Corporation (064437304)
Establishment
NameAddressID/FEIBusiness Operations
Tender Corporation064437304manufacture(44224-0120)

Revised: 3/2017
Document Id: 4aca084a-fc33-360e-e054-00144ff88e88
Set id: 4aca084a-fc32-360e-e054-00144ff88e88
Version: 1
Effective Time: 20170315
 
Tender Corporation