OTC Medication Information: A and D

A AND D — petrolatum ointment
H&H Laboratories, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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

Purpose-Skin Protectant

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.

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.

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

MM1

//otclabels.com/lib/images-otc/a-and-d-1/h-and-h-ad-carton-300x224.jpg
(click image for full-size original)

H and H AD Carton.jpg
A AND D
petrolatum ointment
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:52471-101
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PETROLATUM (PETROLATUM) PETROLATUM 937.5 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
VITAMIN A PALMITATE
ERGOCALCIFEROL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:52471-101-47 144 PACKET (PACKET) in 1 CARTON contains a PACKET (52471-101-05)
1 NDC:52471-101-05 5 g in 1 PACKET This package is contained within the CARTON (52471-101-47)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part347 05/14/2012
Labeler — H&H Laboratories, Inc. (151357175)
Registrant — H&H Laboratories, Inc. (151357175)

Revised: 05/2012 H&H Laboratories, Inc.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Medication Sections

Medication Information by RSS

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2021. All Rights Reserved.