NDC 58264-0030 D-30

NDC Product Code 58264-0030

NDC 58264-0030-1

Package Description: 29.57 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

D-30 with NDC 58264-0030 is a product labeled by Dna Labs, Inc.. The generic name of D-30 is . The product's dosage form is and is administered via form.

Labeler Name: Dna Labs, Inc.

Dosage Form: -

Product Type: 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.

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 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.

D-30 Product Label Images

D-30 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 58264-0030-1

To be used according to standard homeopathic indications.

Otc - Purpose

Stiffness in joints and muscles.

Active

Strontium salicylate 3x, Hexamethyleneimine 4x, Colchicum autumnale 5x, Cimicifuga racemosa 3x, Arnica montana 3x, Calendula officinalis 3x, Dulcamara 3x, Hypericum perforatum 3x, Nux vomica 3x, Belladonna 3x, Echinacea angustifolia 3x, Hamamelis virginiana 3x, Millefolium 3x, Rhus toxicodendron 3x

Inactive

20% alcohol in purified water.

Suggested Dosage

One dropper under tongue two times daily. Acute symptoms ½ dropper under tongue every 30 minutes for two hours.

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.