VITAMIN A D- petrolatum ointment 
Dynarex Corporation

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.

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1152 - Vitamins A&D Ointment, 1 oz tube NDC 67777-214-04
1155 - Vitamins A&D Ointment, 4 oz tube NDC 67777-214-01
1157 - Vitamins A&D Ointment, 15 oz Jar, NDC 67777-214-02

Active Ingredient                               Purpose

White Petrolatum USP (76%)            Skin Protectant

Uses: Vitamin_A_D

Warnings:

For External Use Only

Do Not Get In Eyes

Stop use and ask a doctor if:

Do not use on:

Do not use on:

Keep out of reach of children

Keep out of reach of children

Directions for diaper rash:

Other information:

Inactive Ingredients

Inactive Ingredients: Lanolin, Lavender Oil, Light Liquid Paraffin, Vitamin A, Vitamin D

Indications and Usage

Indications and Usage

A skin protectant for the treatment of diaper rash, minor cuts, scrapes, burns and to help relieve chapped and cracked skin and lips.

1152 IN MASTER

1155 BX MASTER

1157 IN MASTER

VITAMIN A D 
petrolatum ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-214
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM0.76 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
LAVENDER OIL (UNII: ZBP1YXW0H8)  
VITAMIN D (UNII: 9VU1KI44GP)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
LANOLIN (UNII: 7EV65EAW6H)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67777-214-1172 in 1 CASE03/24/2010
1NDC:67777-214-106 in 1 BOX
1NDC:67777-214-01113.4 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:67777-214-0312 in 1 CASE03/24/2010
2NDC:67777-214-02425.25 g in 1 JAR; Type 0: Not a Combination Product
3NDC:67777-214-0672 in 1 CASE03/24/2010
3NDC:67777-214-051 in 1 BOX
3NDC:67777-214-0428.35 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34703/24/2010
Labeler - Dynarex Corporation (008124539)
Registrant - Dynarex Corporation (008124539)

Revised: 11/2022
Document Id: ee14bb7d-aeb9-0661-e053-2995a90af84f
Set id: 62ad33f6-46e6-435f-9a5f-e116c3e218bf
Version: 35
Effective Time: 20221122
 
Dynarex Corporation