AFTER BITE ADVANCED- sodium bicarbonate liquid

After Bite Advanced by

Drug Labeling and Warnings

After Bite Advanced by is a Otc medication manufactured, distributed, or labeled by Tender Corporation d/b/a Adventure Ready Brands. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient / Purpose

Sodium Bicarbonate (Baking Soda) 5% Skin Protectant

Uses

Temproarily protects and helps relieve minor skin irritation and itching due to insect bite poison ivy, oak sumac

Warnings

For external use only.

if in eyes

flush with water for 15 minutes call a doctor

When using this product

do not get into eyes, do not bandage or cover until dry

Stop use and ask a doctor if

condition worsens , symptoms last more than 7 days or clear up and oiccur again within a few days

Keep out of reach of children

if swollowed, get medical help or contact poisin control center right away.

Directions

Adults and children 2 years and older apply to the affected area of the skin as needed or as directed by a doctor

Children under 2 years as a doctor

Inactive Ingredients

Ammonia, glycerin, purified water

Purpose

Skin Protectant

Box artwork

Front of package

Primary label

Label on actual product

INGREDIENTS AND APPEARANCE

AFTER BITE ADVANCED 
sodium bicarbonate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44224-1103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	0.7 g  in 14 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.14 g  in 14 g
AMMONIA (UNII: 5138Q19F1X)	0.778 g  in 14 g
WATER (UNII: 059QF0KO0R)	12.376 g  in 14 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44224-1103-2	1 in 1 BOX	06/17/2025
1	NDC: 44224-1103-0	1 g in 1 VIAL; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	06/17/2025

Labeler - Tender Corporation d/b/a Adventure Ready Brands (064437304)

Establishment
Name	Address	ID/FEI	Business Operations
Tender Corporation d/b/a Adventure Ready Brands		064437304	manufacture(44224-1103)