Label: PETROLATUM ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 59779-148-27 - Packager: CVS
- 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 February 16, 2011
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
Warnings
For external use only.
_______________________________
Do not use on:
- puncture wounds or deep wounds
- animal bites - serious burns
_______________________________
Keep product away from eyes.
_______________________________
Stop use and ask a doctor if:
-condition worsens
-symptoms last more than 7 days; clear
up and occur again within several days
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DOSAGE & ADMINISTRATION
Directions
-for diaper rash:
- change soiled, wet diapers
immediately
- cleanse diaper area thoroughly
and allow to dry
- liberally apply ointment as often as
necessary, with each diaper change,
especially at bedtime or whenever
exposure to wet diapers may be
prolonged
- for other uses: apply as needed
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Other information
Store at 20 degrees to 25 degrees C (68 degrees to 77 degrees F)
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
PETROLATUM
petrolatum ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-148 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 600 mg in 1 g Inactive Ingredients Ingredient Name Strength MINERAL OIL (UNII: T5L8T28FGP) COCOA BUTTER (UNII: 512OYT1CRR) LANOLIN (UNII: 7EV65EAW6H) PARAFFIN (UNII: I9O0E3H2ZE) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) CHOLECALCIFEROL (UNII: 1C6V77QF41) SODIUM PYRUVATE (UNII: POD38AIF08) SUNFLOWER OIL (UNII: 3W1JG795YI) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-148-27 99 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 05/19/2009 Labeler - CVS (062312574) Registrant - Pharma Pac, LLC (140807475) Establishment Name Address ID/FEI Business Operations Pharma Pac, LLC 140807475 manufacture