Label: MEDICATED BODY POWDER- menthol and zinc oxide powder
-
Contains inactivated NDC Code(s)
NDC Code(s): 59240-001-01 - Packager: MAGVERZ INC
- 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 July 15, 2013
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Acitves
- Inactives
- Uses
- Purpose
- Directions
- Warning
- Keep Out of Reach of Childrens
- Product Label
-
INGREDIENTS AND APPEARANCE
MEDICATED BODY POWDER
menthol and zinc oxide powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59240-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.15 g in 100 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 1 g in 100 g Inactive Ingredients Ingredient Name Strength TALC (UNII: 7SEV7J4R1U) Salicylic Acid (UNII: O414PZ4LPZ) ACACIA (UNII: 5C5403N26O) EUCALYPTOL (UNII: RV6J6604TK) METHYL SALICYLATE (UNII: LAV5U5022Y) THYMOL (UNII: 3J50XA376E) ZINC STEARATE (UNII: H92E6QA4FV) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59240-001-01 113 g in 1 CONTAINER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 07/18/2013 Labeler - MAGVERZ INC (078712269) Registrant - MAGVERZ INC (078712269)