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anal GLIDE

Medically reviewed by Drugs.com. Last updated on Jul 29, 2021.

Dosage form: gel
Ingredients: BENZOCAINE 2833mg in 60mL
Labeler: Product Max Group Inc
NDC Code: 70742-092

anal GLIDE - 092

Drug Facts
Active Ingredient

Benzocaine 5%

Purpose

Topical Analgesic

Keep out of reach of children

Keep out of reach of children.

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

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

Warnings

For external use only.

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

Directions
  • When practical, 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

anal GLIDE EXTRA product label

anal GLIDE EXTRA

Desensitizer Lubricating Gel

PREMIUM

Benzocaine Anorectal Gel

Anal Desensitizer

2 FL OZ (60 ml)

www.bodyactionproducts.com

Distributed by:

Body Action Products

Lutz, FL 33559

ACTION BODY PRODUCTS

ANAL GLIDE 
benzocaine gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70742-092
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (BENZOCAINE) BENZOCAINE2833 mg  in 60 mL
Inactive Ingredients
Ingredient NameStrength
HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%) 
METHYLPARABEN 
POLYETHYLENE GLYCOL 400 
PROPYLENE GLYCOL 
PROPYLPARABEN 
WATER 
Packaging
#Item CodePackage Description
1NDC:70742-092-0160 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34806/15/2016
Labeler - Product Max Group Inc (134893911)
Registrant - Product Max Group Inc (134893911)

Document Id: bd0dd8a9-3d50-4b11-bed0-28e5efc99fb7
Set id: 55ac41c4-c0ff-4846-9a6f-39aedbe7d545
Version: 1
Effective Time: 20160808
 
Product Max Group Inc

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer