NDC 81430-0004 Ave Silvergen

Picric Acid

NDC Product Code 81430-0004

NDC 81430-0004-1

Package Description: 100 mL in 1 BOTTLE

NDC Product Information

Ave Silvergen with NDC 81430-0004 is a a human over the counter drug product labeled by Scr Co.,ltd. The generic name of Ave Silvergen is picric acid. The product's dosage form is spray and is administered via topical form.

Labeler Name: Scr Co.,ltd

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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.

Ave Silvergen 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 .0001 g/100mL

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.

Product Labeler Information

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

Labeler Name: Scr Co.,ltd
Labeler Code: 81430
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: 02-11-2021 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: 12-31-2022 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’.

* Please review the disclaimer below.

Ave Silvergen Product Label Images

Ave Silvergen 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

Otc - Active Ingredient

Colloidal nano silver

Inactive Ingredient

Water, gelatin

Otc - Purpose


Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

Take proper amount to the skin


1. For external use only.1) Do not use over the wound and irritated skin with eczema or infections2) Discontinue using the product if signs of irritations and/or rashes occur and seek professional medical help2. Keep the cover closed tight after use3. Do not put the left over contents back into the container to avoid deterioration1) Avoid contact with eyes2) Keep out of reach of children3) Store in a cool and dry place, away from direct sun light

Dosage & Administration

For external use only

* Please review the disclaimer below.