NDC | 0168-0053-16, 0168-0053-21, 0168-0053-31, 0168-0053-45 |
Set ID | b3f48081-1831-401a-b82b-c0cf3ec6697c |
Category | HUMAN OTC DRUG LABEL |
Packager | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART347 |
- Active Ingredient:
- Purpose:
- INDICATIONS & USAGE
- WARNINGS
- Keep out of reach of children.
- DOSAGE & ADMINISTRATION
- SPL UNCLASSIFIED SECTION
- INACTIVE INGREDIENT
- SPL UNCLASSIFIED SECTION
- PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – CONTAINER
- PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – CONTAINER
- PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – CARTON
- PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – CONTAINER
- PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – CARTON
-
INGREDIENTS AND APPEARANCE
WHITE PETROLATUM
white petrolatum ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0168-0053 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 1 g in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0168-0053-16 453.6 g in 1 JAR 2 NDC:0168-0053-21 1 in 1 CARTON 2 28.35 g in 1 TUBE 3 NDC:0168-0053-31 144 in 1 CARTON 3 28.35 g in 1 TUBE 4 NDC:0168-0053-45 1 in 1 CARTON 4 5 g in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 01/01/1968 Labeler - E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. (043838424)