LEGEND AGE WHITENING SUNSCREEN- sunscreen cream

Legend Age Whitening Sunscreen by

Drug Labeling and Warnings

Legend Age Whitening Sunscreen by is a Otc medication manufactured, distributed, or labeled by Guangzhou Fu Zhuang Biotechnology Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS

• For external use only
• When using this product, avoid mouth, nose and eyes
• Stop use and ask a doctor if when the skin feels uncomfortable
• Keep out of touch of children

• Keep out of touch of children.

INACTIVE INGREDIENT

Water, Dipropylene Glycol, Alcohol Denat, 4-Methylbenzylidene Camphor, Glyceryl Stearate, Niacinamide, Pentylene Glycol, Dicaprylyl Carbonate, PEG-100 Stearate, Cyclopentasiloxan, Ethylhexyl Triazone, Panthenol, Polymethylsilsesquioxane, Polysorbate 60, Behenyl Alcohol, Caprylyl Methicone, Triceteareth-4 Phosphate, Glycol Stearate, Pentaerythrityl Distearate, PEG-2 Stearate, Caprylyl Glycol, Glyceryl Caprylate, Silicon Dioxide, Xanthan Gum, Mica, Fragrance(Parfum), Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Glycerin, Isohexadecane, Dimethicone Crosspolymer, PEG-12 Dimethicone Crosspolymer, Polysorbate 80, Disodium EDTA, Sorbitan Oleate, Triethoxycaprylylsilane, Tocopherol, Camellia Japonica Seed Oil, Phenylethyl Resorcinol, Hydrogenated Polydecene, Angelica Gigas Root Extract, Cnidium Officinale Root Extract, Paeonia Lactiflora Root Extract, Rehmannia Glutinosa Root Extract

ACTIVE INGREDIENT

Homosalate 9.5%

Octocrylene 5%

Butyl Methoxydibenzoylmethane 4.5%

Ethylhexyl Salicylate 4.5%

PURPOSE

• helps prevent sunburn
• skin whitening

DOSAGE & ADMINISTRATION

Take an appropriate amount and apply to the skin exposed to the sun (face, neck, arms, hands, legs, back), then even it gently.

INDICATIONS & USAGE

Take an appropriate amount and apply to the skin exposed to the sun (face, neck, arms, hands, legs, back), then even it gently.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LEGEND AGE WHITENING SUNSCREEN 
sunscreen cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82142-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	9.5 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	5 g  in 100 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	4.5 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
HYDROGENATED POLYDECENE (1500 CST) (UNII: 4YI0729529)
NIACINAMIDE (UNII: 25X51I8RD4)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
TOCOPHEROL (UNII: R0ZB2556P8)
CAMELLIA JAPONICA SEED OIL (UNII: U37N0S910T)
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
ALCOHOL (UNII: 3K9958V90M)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
XANTHAN GUM (UNII: TTV12P4NEE)
MICA (UNII: V8A1AW0880)
POLYSORBATE 60 (UNII: CAL22UVI4M)
PENTAERYTHRITYL DISTEARATE (UNII: 697WOT8HNB)
ENZACAMENE (UNII: 8I3XWY40L9)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4)
TRICETEARETH-4 PHOSPHATE (UNII: 69534Y66NO)
GLYCOL STEARATE (UNII: 0324G66D0E)
DOCOSANOL (UNII: 9G1OE216XY)
WATER (UNII: 059QF0KO0R)
PEG-100 STEARATE (UNII: YD01N1999R)
PANTHENOL (UNII: WV9CM0O67Z)
PEG-2 STEARATE (UNII: 94YQ11Y95F)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
GLYCERIN (UNII: PDC6A3C0OX)
ISOHEXADECANE (UNII: 918X1OUF1E)
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
PEG-12 DIMETHICONE/PPG-20 CROSSPOLYMER (UNII: 965K72OQXO)
ANGELICA GIGAS ROOT (UNII: 32766B2FHX)
CNIDIUM OFFICINALE ROOT (UNII: 8S3OZD358J)
PHENYLETHYL RESORCINOL (UNII: G37UFG162O)
PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82142-001-02	1 in 1 BOX	11/18/2021
1	NDC: 82142-001-01	40 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 final	part352	06/23/2021

Labeler - Guangzhou Fu Zhuang Biotechnology Co.,Ltd. (419815629)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Fu Zhuang Biotechnology Co.,Ltd.		419815629	manufacture(82142-001)