Label: SUPRADERM- white petrolatum, lanolin cream
- NDC Code(s): 52358-0002-1, 52358-0002-2, 52358-0002-3
- Packager: Olen Skin Care Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 1, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SUPRADERM
white petrolatum, lanolin creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52358-0002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 0.3 g in 1 g LANOLIN (UNII: 7EV65EAW6H) (LANOLIN - UNII:7EV65EAW6H) LANOLIN 0.15 g in 1 g Inactive Ingredients Ingredient Name Strength ZINC OXIDE (UNII: SOI2LOH54Z) STARCH, CORN (UNII: O8232NY3SJ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52358-0002-1 113 g in 1 JAR; Type 0: Not a Combination Product 11/02/2015 2 NDC:52358-0002-2 340 g in 1 JAR; Type 0: Not a Combination Product 11/02/2015 3 NDC:52358-0002-3 454 g in 1 JAR; Type 0: Not a Combination Product 11/02/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 10/17/2014 Labeler - Olen Skin Care Corporation (250916611)