Label: PHARMACYS PRESCRIPTION PETROLEUM JELLY- petrolatum gel
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Contains inactivated NDC Code(s)
NDC Code(s): 72197-041-06 - Packager: American Consumer Products Corp
- 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 4, 2021
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- Active Ingredients
- Inactive Ingredient
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- Warnings
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INGREDIENTS AND APPEARANCE
PHARMACYS PRESCRIPTION PETROLEUM JELLY
petrolatum gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72197-041 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 99.9 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72197-041-06 170 g in 1 JAR; Type 0: Not a Combination Product 01/22/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 01/22/2021 Labeler - American Consumer Products Corp (081101181)