NDC 48951-2135 Bambusa Argentum

Bambusa Argentum

NDC Product Code 48951-2135

NDC 48951-2135-1

Package Description: 10 BLISTER PACK in 1 BOX > 2 g in 1 BLISTER PACK

NDC Product Information

Bambusa Argentum with NDC 48951-2135 is a a human over the counter drug product labeled by Uriel Pharmacy Inc.. The generic name of Bambusa Argentum is bambusa argentum. The product's dosage form is suppository and is administered via rectal form.

Dosage Form: Suppository - A solid body of various weights and shapes, adapted for introduction into the rectal orifice of the human body; they usually melt, soften, or dissolve at body temperature.

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.

Bambusa Argentum 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.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.


Administration Route(s)

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

  • Rectal - Administration to the rectum.

Product Labeler Information

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

Labeler Name: Uriel Pharmacy Inc.
Labeler Code: 48951
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 09-01-2009 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Bambusa Argentum Product Label Images

Bambusa Argentum 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


Dosage & Administration

Insert 1 suppository as needed.

Otc - Active Ingredient

Active Ingredients: Viscum Mali 4X, Bambusa e nodo 8X, Betonica ex herba 8X, Rosmarinus ex herba 8X, Formica ex animale 9X, Disci intervert. 10X, Jasper 19X, Argentum met. 22X, Arnica e pl. tota 22X

Inactive Ingredient

Inactive Ingredients: Cocoa butter, Sorbitan monolaurate, Micronized silica gel

Otc - Purpose

Use: Temporary relief of headache.

Otc - Keep Out Of Reach Of Children





Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seals on box are broken or missing.

Otc - Questions

Questions? Call 866.642.2858

Uriel, East Troy, WI 53120


* Please review the disclaimer below.