NDC 52471-101 A And D

  1. Labeler Index
  2. H&h Laboratories, Inc.
  3. NDC: 52471-101 A And D

NDC Product Code 52471-101

NDC CODE: 52471-101

Proprietary Name: A And D 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

  • 52471 - H&h Laboratories, Inc.

NDC 52471-101-47

Package Description: 144 PACKET in 1 CARTON > 5 g in 1 PACKET (52471-101-05)

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

NDC Product Information

A And D with NDC 52471-101 is a product labeled by H&h Laboratories, Inc.. The generic name of A And D is . The product's dosage form is and is administered via form.

Labeler Name: H&h Laboratories, 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.
  • VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
  • ERGOCALCIFEROL (UNII: VS041H42XC)

Product Labeler Information

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

Labeler Name: H&h Laboratories, Inc.
Labeler Code: 52471
Start Marketing Date: 05-14-2012 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: 12-31-2017 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.

A And D Product Label Images

A And D 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

Active Ingredient (in each gram): White Petrolatum 93.5%

Otc - Purpose

Purpose-Skin Protectant

Indications & Usage

Uses-Temporarily protects minor cuts, scrapes, and sunburn.     Temporarily protects and helps chapped or cracked skin and lips.  Helps protect lips from drying effects of wind and cold weather.

Dosage & Administration

Directions: Apply liberally as needed  Change wet and soiled diapers promptly.  Cleanse the diaper area and allow to dry. Use with each diaper change, especially at bedtime when exposure to wet diapers may be prolonged.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Warnings

For external use only.  Avoid contact with eyes.  on deep puncture wounds, animal bites, or serious burns. Stop use and ask a doctor if condition worsens, symptoms last for more than 7 days or clear up and occur again within a few days.

Inactive Ingredient

Inactive Ingredients: Corn Oil, Light Mineral Oil, Vitamin A Palmitate, Vitamin D

* Please review the disclaimer below.