NDC 0093-9614 Silver Nitrate

Silver Nitrate

NDC Product Information

Silver Nitrate with NDC 0093-9614 is a a human prescription drug product labeled by Teva Pharmaceuticals Usa, Inc.. The generic name of Silver Nitrate is silver nitrate. The product's dosage form is solution and is administered via topical form.

Labeler Name: Teva Pharmaceuticals Usa, Inc.

Dosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.

Product Type: Human Prescription 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.

Silver Nitrate 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.

  • SILVER NITRATE .005 g/mL

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.

  • WATER (UNII: 059QF0KO0R)

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.
  • 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.

Labeler Name: Teva Pharmaceuticals Usa, Inc.
Labeler Code: 0093
Marketing Category: UNAPPROVED DRUG OTHER - 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: 01-01-1991 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: 12-31-2020 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 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. Values = ‘Y’ or ‘N’.

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Silver Nitrate Product Label Images

Silver Nitrate 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

Silver Nitrate Solution 0.5% 960 Ml Label Text

  • NDC 0093-9614-13Silver NitrateSolution0.5%FOR EXTERNAL USE ONLY.Rx only960 mL (32 fl oz)TEVADESCRIPTION: Silver nitrate solution is a 0.5% solution ofsilver nitrate in a water medium. It is a topical anti-infective.WARNINGS: When ingested, silver nitrate is highly toxic tothe gastrointestinal tract and central nervous system.Swallowing can cause severe gastroenteritis that may endfatally. Sodium chloride may be used by gastric lavage toremove the chemical. Caustic and irritating to the skin andmucous membranes.PRECAUTIONS: Silver nitrate solution must be handled carefully,since it tends to stain the skin, utensils, clothing and linens.DOSAGE: Topical as directed by the physician.Store at 20° to 25°C (68° to 77°F) [See USP ControlledRoom Temperature]. Do not freeze. Protect from light.KEEP THIS AND ALL MEDICATIONS OUT OF THE REACHOF CHILDREN.Manufactured By:HALO PHARMACEUTICALS30 N Jefferson RoadWhippany, NJ 07981Manufactured For:TEVA PHARMACEUTICALS USA, INC.North Wales, PA 19454 333-32-101019Rev. E 2/2016 1021210786-01

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