KISS NEW YORK TINTED MOISTURIZER- zinc oxide cream

KISS New York Tinted Moisturizer by

Drug Labeling and Warnings

KISS New York Tinted Moisturizer by is a Otc medication manufactured, distributed, or labeled by IVY ENTERPRISES, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Stop use and ask doctor if

Do not use :

Keep out of reach of children

Uses - Helps prevent sunburn

Questions contact

Warnings - stop use section

When using

Inactive ingredients

Directions

Warning and precautions

Usage and indications

Front label - Classic tan

INGREDIENTS AND APPEARANCE

KISS NEW YORK TINTED MOISTURIZER 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79906-332
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	3.5 mg  in 100 g

Inactive Ingredients
Ingredient Name	Strength
DIMETHYLSILANOL HYALURONATE (UNII: Z853O1D4TE)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
METHYL TRIMETHICONE (UNII: S73ZQI0GXM)
DIMETHICONE (UNII: 92RU3N3Y1O)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
PALMITOYL PENTAPEPTIDE-4 (UNII: KK181SM5JG)
ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)
TRIPEPTIDE-1 (UNII: 39TG2H631E)
ETHYLHEXYL METHOXYCINNAMATE (UNII: 4Y5P7MUD51)
STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
TOCOPHEROL (UNII: R0ZB2556P8)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0)
CI 77499 (UNII: XM0M87F357)
WATER (UNII: 059QF0KO0R)
DIMETHICONE/POLYGLYCERIN-3 CROSSPOLYMER (UNII: 2P2G24V6T9)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
COPPER TRIPEPTIDE-1 (UNII: 6BJQ43T1I9)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
GLYCERIN (UNII: PDC6A3C0OX)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HYALURONIC ACID (UNII: S270N0TRQY)
HEXAPEPTIDE-9 (UNII: L25414IE41)
SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
POLYGLYCERYL-10 LAURATE (UNII: MPJ2Q8WI8G)
CI 77492 (UNII: EX438O2MRT)
CI 77491 (UNII: 1K09F3G675)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79906-332-00	1 in 1 CARTON	03/24/2025
1	NDC: 79906-332-01	30 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	03/24/2025

Labeler - IVY ENTERPRISES, INC. (832145606)