Label: GG XEROZINE 15- skin protectant ointment
-
Contains inactivated NDC Code(s)
NDC Code(s): 69771-022-23 - Packager: GERI-GENTLE CORPORATION
- 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 December 4, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients:
- Purpose:
- Uses:
- Warnings:
- Warnings:
- Warnings:
- Directions:
- Other Information:
- Inactive Ingredients:
- Label Principal Display Panel
-
INGREDIENTS AND APPEARANCE
GG XEROZINE 15
skin protectant ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69771-022 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 15 g in 100 g DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 1 g in 100 g Inactive Ingredients Ingredient Name Strength ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PETROLATUM (UNII: 4T6H12BN9U) LIGHT MINERAL OIL (UNII: N6K5787QVP) CHOLECALCIFEROL (UNII: 1C6V77QF41) ALOE VERA LEAF (UNII: ZY81Z83H0X) CLOVE LEAF OIL (UNII: VCA5491KVF) LANOLIN (UNII: 7EV65EAW6H) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69771-022-23 113 g in 1 TUBE; Type 0: Not a Combination Product 08/18/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 08/18/2022 Labeler - GERI-GENTLE CORPORATION (080367686)