ARTISTRY SKIN NUTRITION MULTI-DEFENSE UV PROTECT- zinc oxide, titanium dioxide lotion 
Access Business Group LLC

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Artistry Skin Nutrition™ Multi-Defense UV Protect SPF 50

Drug Facts

Active ingredients (w/w)

Zinc Oxide 14.59%

Titanium Dioxide 5.81%

Purpose

Sunscreen

Uses

Warnings

For external use only

Do not use

on broken or damaged skin

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

if rash occurs

Keep out of reach of children.

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

water, propylheptyl caprylate, butyloctyl salicylate, propanediol, C12-15 alkyl benzoate, caprylyl methicone, diphenylsiloxy phenyl trimethicone, acrylates copolymer, polyglyceryl-3 polydimethylsiloxyethyl dimethicone, polyglyceryl-4 diisostearate/polyhydroxystearate/sebacate, vinyl dimethicone/methicone silsesquioxane crosspolymer, pentylene glycol, disteardimonium hectorite, magnesium sulfate, aluminum hydroxide, 1,2-hexanediol, stearic acid, triethoxycaprylylsilane, polyhydroxystearic acid, fragrance, carnosine, iron oxides (ci 77492), isononyl isononanoate, butylene glycol, isododecane, octyldodecanol, ethylhexyl palmitate, isopropyl myristate, isostearic acid, lecithin, dipropylene glycol, polyglyceryl-3 polyricinoleate, iron oxides (ci 77491), iron oxides (ci 77499), polyglyceryl-4 isostearate, salvia hispanica seed extract, punica granatum fruit extract, cynanchum atratum extract, isopropyl titanium triisostearate, tocopherol, chrysanthemum morifolium flower extract, althaea rosea flower extract, ethylhexylglycerin, phenoxyethanol

Questions?

USA: 1-800-253-6500

Package Labeling:

Label

ARTISTRY SKIN NUTRITION MULTI-DEFENSE UV PROTECT 
zinc oxide, titanium dioxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10056-531
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION145.9 mg  in 1 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE58.1 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
PROPANEDIOL (UNII: 5965N8W85T)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
DIPHENYLSILOXY PHENYL TRIMETHICONE (UNII: I445L28B12)  
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)  
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
CARNOSINE (UNII: 8HO6PVN24W)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
ISODODECANE (UNII: A8289P68Y2)  
OCTYLDODECANOL (UNII: 461N1O614Y)  
ETHYLHEXYL PALMITATE (UNII: 2865993309)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
ISOSTEARIC ACID (UNII: X33R8U0062)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)  
CHIA SEED (UNII: NU0OLX06F8)  
POMEGRANATE (UNII: 56687D1Z4D)  
ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)  
TOCOPHEROL (UNII: R0ZB2556P8)  
CHRYSANTHEMUM X MORIFOLIUM FLOWER (UNII: 2GR3C1A0WV)  
ALCEA ROSEA FLOWER (UNII: 1250O8MKPZ)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10056-531-011 in 1 CARTON08/08/2023
150 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02008/08/2023
Labeler - Access Business Group LLC (839830713)

Revised: 10/2023
Document Id: 085c0563-2592-878d-e063-6394a90a43d3
Set id: 82623c46-9ec3-4331-a2db-9b8d07fa1817
Version: 2
Effective Time: 20231023
 
Access Business Group LLC