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Vitamin AD

Dosage form: ointment
Ingredients: PETROLATUM .93g in 1g
Labeler: Dynarex Corporation
NDC Code: 67777-411

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.

Vitamin A D

Active Ingredient                               Purpose

White Petrolatum USP (76%)            Skin Protectant

Purpose:
  • Temporarily protects minor * cuts * scrapes * burns
  • Temporarily helps protect and help relieve chapped and cracked skin and lips
  • Helps prevent and protect from the drying effects of wind and cold weather

Warnings:

For External Use Only

When using this product:
  • Do not get in eyes

Stop use and ask a doctor if:
  • If condition worsens
  • symptoms last more than 7 days or clear up and occur again in a few days

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.

Do Not Use

Do not use on:

  • Deep or puncture wounds
  • animal bites
  • serious burns

Dosage and Administration
  • Apply as needed.

Directions 
  • Apply as needed

Other information:
  • Store at room temperature 15 deg C to 30 deg C    (59 deg F to 86 deg F)
  • Avoid excessive heat and humidity
  • Tamper Evident. Do not use if packet is torn, cut or opened.

Inactive Ingredients:

Inactive Ingredients: Lavender oil, Light Liquid Parafin, Vitamin A, Vitamin D

Principal Display Panel

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VITAMIN AD 
petrolatum ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-411
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PETROLATUM (PETROLATUM) PETROLATUM.93 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
VITAMIN A PALMITATE 
LIGHT MINERAL OIL 
CHOLECALCIFEROL 
LAVENDER OIL 
Packaging
#Item CodePackage Description
1NDC:67777-411-015 g in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34705/10/2015
Labeler - Dynarex Corporation (008124539)
Registrant - Dynarex Corporation (008124539)

 
Dynarex Corporation

Medically reviewed on Apr 5, 2017

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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