Label: AFTER BITE THE ITCH ERASER- sodium bicarbonate liquid
- NDC Code(s): 44224-1030-2
- Packager: Tender Corporation
- 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.
Updated October 27, 2016
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- Drug Facts
- Active Ingredient
For external use only
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
- Inactive Ingredients
Advanced Formula with Baking Soda
Pharmacist Preferred for Insstant Itch Relief!
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- Biting Flies
- Bees & Wasps
- Other Insects
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Satisfaction Guaranteed: Return product to place of purchase or manufacture
Littleton, NH 03561
INGREDIENTS AND APPEARANCE
AFTER BITE THE ITCH ERASER
sodium bicarbonate liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44224-1030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM BICARBONATE (UNII: 8MDF5V39QO) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM BICARBONATE 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength AMMONIA (UNII: 5138Q19F1X) CYCLOMETHICONE 6 (UNII: XHK3U310BA) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:44224-1030-2 1 in 1 BOX 10/01/2014 1 14 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 09/02/2014 Labeler - Tender Corporation (064437304) Establishment Name Address ID/FEI Business Operations Tender Corporation 064437304 manufacture(44224-1030)