AFTER BITE WIPE- sodium bicarbonate swab 
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.

----------

After Bite Wipe

Drug Facts

Active Ingredient

Sodium Bicarbonate (Baking Soda) 5%

Purpose

Skin Protectant

Uses

Temporarily protects and helps relieve minor skin irritation and itching due to

  • Insect bites
  • Poison ivy, oak, or sumac

Warnings

For external use only

Do not use on

  • deep puncture wounds
  • serious burns

When using this product

avoid contact with eyes. Do not bandage or cover until dry.

Stop use and ask a doctor If

  • conditions worsens
  • symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

Directions

  • Adults and children 2 years and older dab directly on bite or sting, rub gently and re-apply as needed
  • Children under 2 years ask a doctor

Inactive Ingredients

Ammonia, Cyclohexasiloxane, Cyclopentasiloxane, Glycerin, Purified Water

After Bite

After Bite Wipe

AFTER BITE WIPE 
sodium bicarbonate swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44224-3622
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM BICARBONATE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
AMMONIA (UNII: 5138Q19F1X)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:44224-3622-00.74 mL in 1 POUCH; Type 0: Not a Combination Product07/01/201909/30/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34707/01/201909/30/2022
Labeler - Tender Corporation (064437304)
Registrant - Tender Corporation (064437304)
Establishment
NameAddressID/FEIBusiness Operations
Tender Corporation064437304manufacture(44224-3622)

Revised: 1/2021
 
Tender Corporation