BODY ACTION PRODUCTS ANAL GLIDE EXTRA- benzocaine gel

BODY ACTION PRODUCTS Anal Glide Extra by

Drug Labeling and Warnings

BODY ACTION PRODUCTS Anal Glide Extra by is a Otc medication manufactured, distributed, or labeled by PRODUCT MAX GROUP INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Benzocaine 5%

Purpose

Anorectal (Hemorrhoidal) Gel

Uses

• For temporary relief of pain or soreness in the perianal area.

Warnings

For external use only.

• Avoid contact with the eyes.
• Certain persons can develop allergic reactions from ingredients in this product. If the symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase, discontinue use and consult a doctor.

Keep out of reach of children.

If swallowed get medical help or contact a Poison Control Center right away.

Directions

• When practial, cleanse the affected area with mild soap and warm water and rinse thoroughly.
• Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product.
• Apply to the affected area up to 6 times daily.

Other Information

Do not use if safety seal is broken or missing.

Inactive Ingredients

Hydroxyethylcellulose, Methylparaben, PEG-8, Propylene Glycol, Propylparaben, Water.

Package Labeling:

INGREDIENTS AND APPEARANCE

BODY ACTION PRODUCTS ANAL GLIDE EXTRA 
benzocaine gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70742-287
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
METHYLPARABEN (UNII: A2I8C7HI9T)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70742-287-00	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/29/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M015	04/29/2022

Labeler - PRODUCT MAX GROUP INC (134893911)