Label: BABY PETROLATUM JELLY- petrolatum jelly
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Contains inactivated NDC Code(s)
NDC Code(s): 52410-0206-2, 52410-0206-4 - Packager: SHIELD LINE LLC
- 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 24, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings: FOR EXTERNAL USE ONLY
- When using this product
- Stop Use and ask a doctor if
- Keep out of reach of children
- Directions
- Other Information
- Inactive Ingredient
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BABY PETROLATUM JELLY
petrolatum jellyProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52410-0206 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:52410-0206-2 226 g in 1 JAR; Type 0: Not a Combination Product 06/21/2016 2 NDC:52410-0206-4 368 g in 1 JAR; Type 0: Not a Combination Product 06/21/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 06/21/2016 Labeler - SHIELD LINE LLC (078518916)