After Bite Advanced by Adventure Ready Brands After Bite Advanced

After Bite Advanced by

Drug Labeling and Warnings

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

Drug Details [pdf]

AFTER BITE ADVANCED- sodium bicarbonate liquid 
Adventure Ready Brands

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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After Bite Advanced

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

• 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

If in eyes

flush with water for 15 minutes and call a doctor

Directions

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

Inactive Ingredients

Ammonia, Cyclohexasiloxane, Cyclopentasiloxane, Glycerin, Purified Water

After Bite

AFTER BITE ADVANCED 
sodium bicarbonate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 90107-1030
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: 90107-1030-1	1 in 1 BOX	09/01/2020	12/31/2023
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	09/01/2020	12/31/2023

Labeler - Adventure Ready Brands (064437304)

Registrant - Adventure Ready Brands (064437304)

Establishment
Name	Address	ID/FEI	Business Operations
Adventure Ready Brands		064437304	manufacture(90107-1030)

Revised: 1/2021

Document Id: b982b333-7ad6-c7a5-e053-2a95a90af3b0

34390-5

Set id: af99f49e-c06e-093c-e053-2a95a90a7821

Version: 2

Effective Time: 20210122