VITAMIN AD- petrolatum ointment

Vitamin AD by

Drug Labeling and Warnings

Vitamin AD by is a Otc medication manufactured, distributed, or labeled by Dynarex Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

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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INGREDIENTS AND APPEARANCE

VITAMIN AD 
petrolatum ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-411
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	.93 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
LIGHT MINERAL OIL (UNII: N6K5787QVP)
CHOLECALCIFEROL (UNII: 1C6V77QF41)
LAVENDER OIL (UNII: ZBP1YXW0H8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-411-01	5 g in 1 PACKET; Type 0: Not a Combination Product	04/05/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	05/10/2015

Labeler - Dynarex Corporation (008124539)

Registrant - Dynarex Corporation (008124539)