NDC 52471-101 A And D

Product Information

A And D is product labeled by H&h Laboratories, Inc.. The product's dosage form is and is administered via form.

Product Code52471-101
Proprietary Name 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.
A And D
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
H&h Laboratories, Inc.
Labeler Code52471
Start Marketing Date 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 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 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".
NDC Code Structure

What are the uses for A And D?

Product Packages

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.

Product Details

What are A And D Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
  • PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)

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.

* Please review the disclaimer below.

A And D Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents

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.


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

Package Label.Principal Display Panel


* Please review the disclaimer below.