Label: NOVITA BABY PETROLATUM JELLY- petrolatum jelly
- NDC Code(s): 52410-1021-3, 52410-1021-5
- 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 January 12, 2023
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- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Do not use on
- Keep out of reach of children
- Directions
- Inactive Ingredient
- Package Label
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INGREDIENTS AND APPEARANCE
NOVITA BABY PETROLATUM JELLY
petrolatum jellyProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52410-1021 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:52410-1021-3 226 g in 1 JAR; Type 0: Not a Combination Product 10/11/2016 2 NDC:52410-1021-5 368 g in 1 JAR; Type 0: Not a Combination Product 10/11/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 10/11/2016 Labeler - Shield Line LLC (078518916)