Otc - Active Ingredient
Active Ingredient (in each gram): White Petrolatum 93.5%
A And D
FDA Label NDC 52471-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by H&h Laboratories, Inc. for the product A And D (NDC 52471-101). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, dosage & administration, otc - keep out of reach of children, warnings, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
Package Label.Principal Display Panel
MM1
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