AFTER BITE THE ITCH ERASER- sodium bicarbonate liquid

After Bite the Itch Eraser by

Drug Labeling and Warnings

After Bite the Itch Eraser by is a Otc medication manufactured, distributed, or labeled by Tender Corporation. 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

Do not use on

• deep puncture wounds
• serious burns

When using this product

• do not get into eyes

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 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

Advanced Formula with Baking Soda

Pharmacist Preferred for Insstant Itch Relief!

Be Ready For:

• Mosquitoes
• Biting Flies
• Bees & Wasps
• Other Insects

After Bite's advanced formula with baking soda now provides better relief for the whole family.

After Bite akes it easy to instantly stop the itch or sting wherever you are...a hike, the beach, or in your backyard. Don't let insects ruin your family fun!

See our complete line of products at AfterBite.com

Insectlopedia.com your source for treatment, prevention, and the latest "buzz" on bugs

Satisfaction Guaranteed: Return product to place of purchase or manufacture

Tender Corporation

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)