Label: MENTHOL AND ZINC OXIDE ointment
-
Contains inactivated NDC Code(s)
NDC Code(s): 77338-013-23 - Packager: ASTONEA LABS PRIVATE LIMITED
- Category: HUMAN OTC DRUG LABEL
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 August 17, 2022
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- uses
- Warnings:
- Stop use and ask a doctor if
- Keep Out Of Reach Of Children
- Dosage & Administration:
- Inactive Ingredients
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
MENTHOL AND ZINC OXIDE
menthol and zinc oxide ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77338-013 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.44 g in 100 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 20.625 g in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) FERRIC OXIDE RED (UNII: 1K09F3G675) LANOLIN (UNII: 7EV65EAW6H) LIGHT MINERAL OIL (UNII: N6K5787QVP) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) THYMOL (UNII: 3J50XA376E) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77338-013-23 113 g in 1 TUBE; Type 0: Not a Combination Product 08/17/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 08/17/2022 Labeler - ASTONEA LABS PRIVATE LIMITED (878533295)