Label: GZE TINTED SUNSCREEN- zinc oxide 3% cream
- NDC Code(s): 83566-101-01
- Packager: Guangdong Aimu Biological Technology Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 20, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- WARNINGS
- DO NOT USE
-
WHEN USING
Super-Light Daily Wrinkle Defense
INSTANTLY OBTAIN seemingly flawless, glowingskin. Perfect for that no-make up look.FORMULATED AS AN ALLIN ONE SUNSCREEN ANDFOUNDATION that provides sheer color coverage,minimizes the appearance of fine lines andwrinkles, and blends naturally to match every skintone.LIGHTWEIGHT AND NON-GREASY FORMULA thatimproves your skin's hydration and texture over
time. - STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
-
INACTIVE INGREDIENT
Water
Polydimethylsiloxane
Peg Ppg-1818polydimethylsiloxane
DIMETHICONE
PEG-12 DIMETHICONE
Resveratrol
SOY ISOFLAVONES
Epicatechin
Tocopherol Acetate
ASCORBYL TETRAISOPALMITATE
Adenosine
LAUROYL LYSINE
Red Myrrh Alcohol
TRIHYDROXYSTEARIN
Barkextract Of Salixalba
Pomegranate Extract
Haematococcus Pluvialis Extract
Hydrolyzedcorn Starch
Polysorbate-80
Silica Triethoxy Octylsilane
C12-15 Alcohol Benzoate
Triisostearic Acidisopropyl Titanium Salt
Octanol
Hexanediol
Sodium Argon
Ethyl Hexyl Glycerol
2-Phenoxyethanol
Iron Oxide - PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
GZE TINTED SUNSCREEN
zinc oxide 3% creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83566-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 3 mg in 100 mL Inactive Ingredients Ingredient Name Strength ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A) LAUROYL LYSINE (UNII: 113171Q70B) LEVOMENOL (UNII: 24WE03BX2T) TRIHYDROXYSTEARIN (UNII: 06YD7896S3) SALIX ALBA BARK (UNII: 205MXS71H7) HAEMATOCOCCUS PLUVIALIS (UNII: 31T0FF0472) POLYSORBATE 80 (UNII: 6OZP39ZG8H) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) FERRIC OXIDE RED (UNII: 1K09F3G675) PEG-12 DIMETHICONE (UNII: ZEL54N6W95) RESVERATROL (UNII: Q369O8926L) SOY ISOFLAVONES (UNII: 71B37NR06D) EPICATECHIN (UNII: 34PHS7TU43) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ADENOSINE (UNII: K72T3FS567) POMEGRANATE (UNII: 56687D1Z4D) CAPRYLIC ALCOHOL (UNII: NV1779205D) HEXANEDIOL (UNII: ZIA319275I) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) MALTOTETRAOSE (UNII: BO88JLT87R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I) PHENOXYETHANOL (UNII: HIE492ZZ3T) WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) EDETATE DISODIUM (UNII: 7FLD91C86K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83566-101-01 40 mL in 1 TUBE; Type 0: Not a Combination Product 07/07/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 07/07/2023 Labeler - Guangdong Aimu Biological Technology Co., Ltd (712647107) Registrant - Guangdong Aimu Biological Technology Co., Ltd (712647107) Establishment Name Address ID/FEI Business Operations Guangdong Aimu Biological Technology Co., Ltd 712647107 manufacture(83566-101)
