Label: PETROLEUM JELLY- white petrolatum jelly
-
Contains inactivated NDC Code(s)
NDC Code(s): 0363-0721-01 - Packager: Walgreens
- 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, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- When using this product
- See a doctor if
- Do not use on
- Keep out of reach of children.
- Directions
- Label
-
INGREDIENTS AND APPEARANCE
PETROLEUM JELLY
white petrolatum jellyProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0721 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 Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0721-01 50 g in 1 JAR; Type 0: Not a Combination Product 02/04/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 02/04/2018 Labeler - Walgreens (008965063) Establishment Name Address ID/FEI Business Operations Unipack, Inc. 009248480 manufacture(0363-0721)