NDC 58264-0013 D-13

NDC Product Code 58264-0013

NDC 58264-0013-1

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-13 with NDC 58264-0013 is a product labeled by Dna Labs, Inc.. The generic name of D-13 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.

D-13 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 58264-0013-1

  • Use only if cap seal is unbroken.

To be used according to standard homeopathic indications.

Otc - Purpose

Hemorrhoids, itching, pains.

Active

Aesculus hippocastanum 2x, Hamamelis virginiana 3x, Paeonia officinalis 3x, Nux vomica 4x, Graphites 8x, Sulphur 5x, Collinsonia canadensis 4x, Kalium carbonicum 6x, Lycopodium clavatum 5x, Acidum nitricum 6x

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

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.