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Body action products anal glide extra - Medication Information

Product NDC Code 70742-287
Drug Name

Body action products anal glide extra

Type Brand
Pharm Class Allergens [CS],
Cell-mediated Immunity [PE],
Increased Histamine Release [PE],
Standardized Chemical Allergen [EPC]
Active Ingredients
Benzocaine 50 mg/ml
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 2599842
Application Number M015
Labeler Name PRODUCT MAX GROUP INC
Packages
Package NDC Code Description
70742-287-00 60 ml in 1 bottle (70742-287-00)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Benzocaine 5% Purpose Anorectal (Hemorrhoidal) Gel

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
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.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Hydroxyethylcellulose, Methylparaben, PEG-8, Propylene Glycol, Propylparaben, Water.

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses For temporary relief of pain or soreness in the perianal area.

Purpose

Information about the drug product’s indications for use.
Purpose Anorectal (Hemorrhoidal) Gel

Spl product data elements

Usually a list of ingredients in a drug product.
BODY ACTION PRODUCTS Anal Glide Extra BENZOCAINE HYDROXYETHYL CELLULOSE, UNSPECIFIED METHYLPARABEN POLYETHYLENE GLYCOL 400 PROPYLENE GLYCOL PROPYLPARABEN WATER BENZOCAINE BENZOCAINE

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Package Labeling: Label2

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Drug Facts Other Information Do not use if safety seal is broken or missing.

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
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.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API