SUNTAN- suntan lotion cream, augmented

Suntan by

Drug Labeling and Warnings

Suntan by is a Homeopathic medication manufactured, distributed, or labeled by Guangzhou shangwei Beauty TechnologyCo.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

OTC-ACTIVE INGREDIENT SECTION

OTC-ACTIVE INGREDIENT SECTION:Water,

OTC-PURPOSR SECTION

OTC - PURPOSE SECTION

OTC-KEEP OUT OF REACH OF CHILDREN SECTION

OTC-KEEP OUT OF REACH OF CHILDREN SECTION:To avoid danger of suffocation keep this bag away from babies and children Do not use this bag in cribs,beds carriages or play pens.this bag is not a toy.

INDICATIONS

1.For external use only,Avoid contact with eyes.

2.Keep away from babies and children.

3.If feel any discomfort after use，please stop using it

4.Keep away from fire sources and direct sunlight

WARNINGS SECTION

To avoid danger of suffocation keep this bag away from babies and children.Do not use this bag in cribs beds,besd,cariages,or play pens.this bag is not a toy.

DOSAGE

ERROR HAS OCCURRED 1g

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION :Oryza Sativa (Rice),Dibutyl Adipate,Propanediol,Diethylamino Hydroxybenzoyl Hexyl Benzoate,Polymethylsilsesquioxane,Ethylhexyl Triazone,Niacinamide,Methylene Bis-Benzotriazolyl Tetramethylbutylphenol,Coco-Caprylate/Caprate,Diethylhexyl Butamido Triazone,Glycerin,Butylene Glycol,Decyl Glucoside,Tromethamine,Carbomer.1,2-Hexanediol,Disodium Stearoyl Glutamate,Polyacrylate Crosspolymer-6,Ethylhexylglycerin,Adenosine,Xanthan Gum,Tocopherol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SUNTAN 
suntan lotion cream, augmented

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85421-001
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R)	WATER	50 g  in 100

Inactive Ingredients
Ingredient Name	Strength
TROMETHAMINE (UNII: 023C2WHX2V)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4)
METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL (UNII: 8NT850T0YS)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
PROPANEDIOL (UNII: 5965N8W85T)
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
TOCOPHEROL (UNII: R0ZB2556P8)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
NIACINAMIDE (UNII: 25X51I8RD4)
POLYACRYLATE CROSSPOLYMER-6 (UNII: Q7UI015FF9)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)
DIETHYLHEXYL BUTAMIDO TRIAZONE (UNII: 2UTZ0QC864)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
ORYZA SATIVA (RICE) HULL POWDER (UNII: C6HBM3R8DB)
ADENOSINE (UNII: K72T3FS567)
XANTHAN GUM (UNII: TTV12P4NEE)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
GLYCERIN (UNII: PDC6A3C0OX)
BEHENYL ALCOHOL (UNII: 9G1OE216XY)
DIBUTYL ADIPATE (UNII: F4K100DXP3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85421-001-00	1 in 1 BOX, UNIT-DOSE	03/22/2025
1		1 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		03/22/2025

Labeler - Guangzhou shangwei Beauty TechnologyCo.,Ltd. (704798510)