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
Drug Label Information
Updated November 20, 2024
If you are a consumer or patient please visit this version.
- 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 Drug M016 03/24/2010 Labeler - Dynarex Corporation (008124539) Registrant - Dynarex Corporation (008124539)



