SEXY MIX TATTOO ULTRA SUNSCREEN BROAD SPECTRUM SPF 50- avobenzone, homosalate, octisalate, octocrylene cream

SEXY MIX Tattoo Ultra Sunscreen Broad Spectrum SPF 50 by

Drug Labeling and Warnings

SEXY MIX Tattoo Ultra Sunscreen Broad Spectrum SPF 50 by is a Otc medication manufactured, distributed, or labeled by Aopline Health Industry Technology (Guangzhou) Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Avobenzone 3%
Homosalate 5%
0ctisalate 5%
0ctocrylene 10%

Purpose

purpose: sunscreen

Uses

Uses
Helps prevent sunburn
Higher SPF gives more sunburn protection
If used as directed with other sun protection
measures ( see Directions ) , decreases the risk of skin
cancer and early skin aging caused by the sun

Warnings

Warnings
For external use only .
y on damaged or broken 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 swallowed , get
medical help or contact a Poison Control Center right
away .

Directions

Directions
Apply liberally 15 minutes before sun exposure
Reapplly :
After 80 minutes of swimming or sweating
Immediately after towel drying
At least every 2 hours
Children under 6 months of age : ask a doctor
Sun Protection Measures . Spending time in the sun
increases your risk of skin cancer and early skin aging
To decrease this risk , regularly use a sunscreen with a
broad-spectrum SPF of 15 or higher and other sun
protection measures including :
Limit time in the sun , especially from 10 a m . -2 p m
Wear long-sleeve shirts , pants , hats , and sunglasses .

Other Information

Other information
protect this product from excessive heat and direct sun

Inactive Ingredients

Inactive ingredients
Aqua, Propylene Glycol, Glycerin, Inulin Laury
Carbamate, Vinyl Dimethicone/Methicone
Silsesquioxane Crosspolymer, Cetearyl Alcohol,
Potassium Cetyl Phosphate, Sodium Polyacrylate,
Ethylhexyl Stearate, Trideceth-6, Ammonium
Acryloyldimethyltaurate/Vp Copolymer,
Phenoxyethanol, 1, 2-hexanediol
Hydroxyacetophenone, Maltodextrin, Centella
Asiatica Leaf Extract Aloe Barbadensis Leaf Water
Saccharomyces/ice Ferment Filtrate, Butylene
Glycol, Anhydroxylitol, Tremella Fuciformis
(Mushroom)Extract, Centella Asiatica Extract, Xylitol

Keep out of reach of children.

Keep out of reach of children . If swallowed , get
medical help or contact a Poison Control Center right
away .

Stop use

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

WHEN USING

When using this product keep out of eyes , Rinse
with water to remove
Stop use and ask a doctor if rash occurs

Do not use

Do not use on damaged or broken 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 swallowed , get medical
help or contact a Poison Control Center right away .

Package Label

82723-005 TATTOO ULTRA SUNSCREEN

INGREDIENTS AND APPEARANCE

SEXY MIX TATTOO ULTRA SUNSCREEN BROAD SPECTRUM SPF 50 
avobenzone, homosalate, octisalate, octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82723-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 mg  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	5 mg  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 mg  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	10 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
XYLITOL (UNII: VCQ006KQ1E)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
ANHYDROXYLITOL (UNII: 8XWR7NN42F)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CENTELLA ASIATICA LEAF (UNII: 6810070TYD)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
INULIN LAURYL CARBAMATE (UNII: 48RFF58ESG)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82723-005-01	90 mL in 1 BOX; Type 0: Not a Combination Product	11/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/01/2023

Labeler - Aopline Health Industry Technology (Guangzhou) Co., Ltd. (715076108)

Establishment
Name	Address	ID/FEI	Business Operations
Aopline Health Industry Technology (Guangzhou) Co., Ltd.		715076108	manufacture(82723-005)