Label: VITAMIN A D- petrolatum ointment
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NDC Code(s):
67777-214-01,
67777-214-02,
67777-214-03,
67777-214-04, view more67777-214-05, 67777-214-06, 67777-214-10, 67777-214-11
- Packager: Dynarex Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 Label Information
Updated November 22, 2022
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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Uses: Vitamin_A_D
- Helps treat and prevent diaper rash
- Helps seal out wetness
- 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
- Helps prevent and protect chafed skin or minor skin irritations associated with diaper rash
- With each diaper change, especially at bedtime when exposure to wet diapers may be prolonged
- Warnings:
- Stop use and ask a doctor if:
- Do not use on:
- Keep out of reach of children
- Directions for diaper rash:
- Other information:
- Inactive Ingredients
- Indications and Usage
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
VITAMIN A D
petrolatum ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67777-214 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 0.76 g in 1 g Inactive Ingredients Ingredient Name Strength LAVENDER OIL (UNII: ZBP1YXW0H8) VITAMIN D (UNII: 9VU1KI44GP) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) LANOLIN (UNII: 7EV65EAW6H) LIGHT MINERAL OIL (UNII: N6K5787QVP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67777-214-11 72 in 1 CASE 03/24/2010 1 NDC:67777-214-10 6 in 1 BOX 1 NDC:67777-214-01 113.4 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:67777-214-03 12 in 1 CASE 03/24/2010 2 NDC:67777-214-02 425.25 g in 1 JAR; Type 0: Not a Combination Product 3 NDC:67777-214-06 72 in 1 CASE 03/24/2010 3 NDC:67777-214-05 1 in 1 BOX 3 NDC:67777-214-04 28.35 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 03/24/2010 Labeler - Dynarex Corporation (008124539) Registrant - Dynarex Corporation (008124539)