AFTER BITE X TECH- sodium bicarbonate liquid

After Bite X Tech by

Drug Labeling and Warnings

After Bite X Tech by is a Otc medication manufactured, distributed, or labeled by Adventure Ready Brands. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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 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.

If in eyes

flush with water for 15 minutes and call a doctor.

Directions

• Adults and children 2 years and older firmly press X-Applicator to the affected area of the skin to apply liquid as needed or as directed by a doctor.
• Children under 2 years ask a doctor.

Inactive Ingredients

Ammonia, Glycerin, Purified Water

After Bite X Tech Vial Label

after Bite X Tech Box

INGREDIENTS AND APPEARANCE

AFTER BITE X TECH 
sodium bicarbonate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44224-1040
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 1000 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
AMMONIA (UNII: 5138Q19F1X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44224-1040-1	1 in 1 BOX	11/15/2024
1		14 mL in 1 TUBE, WITH APPLICATOR; 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	01/01/2023

Labeler - Adventure Ready Brands (064437304)

Registrant - Adventure Ready Brands (064437304)

Establishment
Name	Address	ID/FEI	Business Operations
Adventure Ready Brands		064437304	manufacture(44224-1040) , label(44224-1040) , pack(44224-1040)