Label: PETROLEUM JELLY BABY DAYS- petrolatum jelly
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Contains inactivated NDC Code(s)
NDC Code(s): 22431-133-01 - Packager: Blue Cross Laboratories, Inc.
- 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 13, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PETROLEUM JELLY BABY DAYS
petrolatum jellyProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:22431-133 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 100 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:22431-133-01 170 g in 1 JAR; Type 0: Not a Combination Product 01/25/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 01/25/2019 Labeler - Blue Cross Laboratories, Inc. (008298879) Registrant - Blue Cross Laboratories, Inc (008298879) Establishment Name Address ID/FEI Business Operations ROYAL EXPORTS 650621381 manufacture(22431-133) Establishment Name Address ID/FEI Business Operations Jell Pharmaceuticals Private Limited 726025211 manufacture(22431-133)
