ARTISTRY SKIN NUTRITION HYDRATING DAY- avobenzone, octisalate, octocrylene lotion

Artistry Skin Nutrition HYDRATING Day by

Drug Labeling and Warnings

Artistry Skin Nutrition HYDRATING Day by is a Otc medication manufactured, distributed, or labeled by Access Business Group LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients (w/w)

Avobenzone 3% Octisalate 5% Octocrylene 7%

Purpose

Sunscreen

Uses

Helps prevent sunburn

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

For sunscreen use

• Apply liberally 15 minutes before sun exposure
• Use a water resistant sunscreen if swimming or sweating or washing
• Reapply at least every 2 hours
• Children under 6 months: ask a doctor

Other information

• Protect this product from excessive heat and direct sun

Inactive ingredients

water, dimethicone, propanediol, butyloctyl salicylate, cetearyl alcohol, glycerin, polysorbate 80, butylene glycol, ammonium acryloyldimethyltaurate/ VP copolymer, phenoxyethanol, salvia hispanica seed oil, calcium sodium borosilicate, cetearyl glucoside, tocopheryl acetate, chlorphenesin, malpighia emarginata (acerola) fruit extract, pentylene glycol, allantoin, carnosine, dipotassium glycyrrhizate, fragrance/parfum, dipropylene glycol, disodium EDTA, isononyl isononanoate, , tocopherol, glycine soja (soybean) oil, maltodextrin, citric acid, lecithin, centipeda cunninghamii extract, pentadecalactone, salvia hispanica seed extract, carrageenan, punica granatum fruit extract, zinc PCA, rubus fruticosus (blackberry) leaf extract, ceramide NP, sea salt, beta-sitosterol, sodium hyaluronate, oenothera biennis (evening primrose) oil, perilla ocymoides seed oil, helianthus annuus (sunflower) seed oil, BHT

Questions?

USA: 1-800-253-6500

Package Labeling:

INGREDIENTS AND APPEARANCE

ARTISTRY SKIN NUTRITION HYDRATING DAY 
avobenzone, octisalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10056-041
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	70 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
PROPANEDIOL (UNII: 5965N8W85T)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
GLYCERIN (UNII: PDC6A3C0OX)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CHIA SEED OIL (UNII: MC2LH51BO7)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CHLORPHENESIN (UNII: I670DAL4SZ)
ACEROLA (UNII: XDD2WEC9L5)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
ALLANTOIN (UNII: 344S277G0Z)
CARNOSINE (UNII: 8HO6PVN24W)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
TOCOPHEROL (UNII: R0ZB2556P8)
SOYBEAN OIL (UNII: 241ATL177A)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
PENTADECALACTONE (UNII: OK17S3S98K)
CARRAGEENAN (UNII: 5C69YCD2YJ)
POMEGRANATE (UNII: 56687D1Z4D)
ZINC PIDOLATE (UNII: C32PQ86DH4)
RUBUS FRUTICOSUS LEAF (UNII: YQ2S06L8S9)
CERAMIDE NP (UNII: 4370DF050B)
SEA SALT (UNII: 87GE52P74G)
.BETA.-SITOSTEROL (UNII: S347WMO6M4)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
PERILLA FRUTESCENS SEED OIL (UNII: 322MS57V7Z)
SUNFLOWER OIL (UNII: 3W1JG795YI)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10056-041-00	1 in 1 CARTON	04/04/2021
1		50 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	04/04/2021

Labeler - Access Business Group LLC (839830713)