A and D plus E

Dosage form: ointment
Ingredients: PETROLATUM 937.5mg in 1g
Labeler: H&H Laboratories, Inc.
NDC Code: 52471-100

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.

DRUG FACTS

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

Purpose-Skin Protectant

Uses-Temporarily protects minor cuts, scrapes, and sunburn.     Helps treat and prevent diaper rash.  Protects chafed skin or minor skin irritation associated with diaper rash and helps seal out wetness. 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.  Do not use in eyes, on deep puncture wounds, animal bites, or serious burns or for more than 1 week unless directed by a doctor.

Stop use and ask a doctor if: A rash or allergic reaction develops.  Condition worsens, persists, or recurs.

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

MM1

MM2




A AND D PLUS E 
petrolatum ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52471-100
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PETROLATUM (PETROLATUM) PETROLATUM937.5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
VITAMIN A PALMITATE 
ERGOCALCIFEROL 
Packaging
#Item CodePackage Description
1NDC:52471-100-04113 g in 1 TUBE
2NDC:52471-100-13168 g in 1 JAR
3NDC:52471-100-16454 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34705/14/2012
Labeler - H&H Laboratories, Inc. (151357175)
Registrant - H&H Laboratories, Inc. (151357175)

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

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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