NDC 48951-2132 Bismuth Stibium

Bismuth Stibium

NDC Product Code 48951-2132

NDC Product Information

Bismuth Stibium with NDC 48951-2132 is a a human over the counter drug product labeled by Uriel Pharmacy Inc.. The generic name of Bismuth Stibium is bismuth stibium. The product's dosage form is ointment and is administered via topical form.

Labeler Name: Uriel Pharmacy Inc.

Dosage Form: Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.


Bismuth Stibium Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • GARLIC 1 [hp_X]/g
  • CHELIDONIUM MAJUS 1 [hp_X]/g
  • TURMERIC 1 [hp_X]/g
  • THUJA OCCIDENTALIS WHOLE 1 [hp_X]/g
  • BISMUTH 2 [hp_X]/g
  • ANTIMONY 2 [hp_X]/g

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

* Please review the disclaimer below.

Bismuth Stibium Product Label Images

Bismuth Stibium Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Indications & Usage

Directions: FOR TOPICAL USE ONLY.

Dosage & Administration

Apply once or twice daily to warts. Under age 2: Consult a doctor

Otc - Active Ingredient

Active Ingredients: 100 gm contains: 25 gm Allium sativa (Garlic) 1X, 25 gm Chelidonium (Greater celandine) 1X, 25 gm Curcuma (Turmeric) 1X, 25 gm Thuja (American arborvitae) 1X, 20 gm Bismuth 2X, 20 gm Stibium met. (Antimony) 2X

Inactive Ingredient

Inactive Ingredients: White petrolatum, Lanolin, Mineral oil, Glyceryl monostearate, Potassium sorbate, Grapefruit seed extract

Otc - Purpose

Use: Temporary relief of warts.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Warnings

Warnings: FOR EXTERNAL USE ONLY. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing.

Otc - Questions

Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI 53120 www.urielpharmacy.com

* Please review the disclaimer below.

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