NDC 58264-0395 G-32

  1. Labeler Index
  2. Dna Labs, Inc.
  3. NDC: 58264-0395 G-32

NDC Product Code 58264-0395

NDC CODE: 58264-0395

Proprietary Name: G-32 What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

NDC 58264-0395-2

Package Description: 59.14 mL in 1 BOTTLE, GLASS

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

G-32 with NDC 58264-0395 is a product labeled by Dna Labs, Inc.. The generic name of G-32 is . The product's dosage form is and is administered via form.

Labeler Name: Dna Labs, Inc.

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.
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Dna Labs, Inc.
Labeler Code: 58264
Start Marketing Date: 01-01-1990 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: 12-31-2019 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

G-32 Product Label Images

G-32 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

Other

NDC 58264-0395-2

To be used according to standard homeopathic indications.

Otc - Purpose

General allergies, supports the liver and colon.

Active

Rosmarinus officinalis (Rosemary) 1DH

Inactive

36.6% alcohol (V/V) Glycerin Macerate

Suggested Dosage

One dropper full twice daily.

Storage And Handling

SHAKE WELL

Warnings

  • Use only if cap seal is unbroken.

Otc - Pregnancy Or Breast Feeding

  • If pregnant or breastfeeding, ask a healthcare professional before use.

Otc - Keep Out Of Reach Of Children

  • Keep this and all medication out of the reach of children.

* Please review the disclaimer below.