SUN SCREENLOTION SPF30 01- octinoxate,avobenzone,oxybenzone,titanium dioxide lotion

SUN SCREENLOTION SPF30 by

Drug Labeling and Warnings

SUN SCREENLOTION SPF30 by is a Otc medication manufactured, distributed, or labeled by Shenzhen Lantern Scicence Co.,Ltd., LANTERN HEALTH&BEAUTY LAB INC., Shenzhen Lantern Science Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

ETHYLHEXYL METHOXYCINNAMATE：8.5%

Avobenzone：3.0%

Titanium dioxide：3.0%

Sunscreen

Inactive ingredients

AQUA, METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHE NOL, AQUA, DECYL GLUCOSIDE, PROPYLENE GLYCOL, XANTHAN GUM, GLYCERIN, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, ETHYLHEXYL TRIAZONE, DIMETHICONE, PEG-20 METHYL GLUCOSE SESQUISTEARATE, AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER, METHYL GLUCOSE SESQUISTEARATE, PHENOXYETHANOL, TOCOPHERYL ACETATE, PARFUM, MENTHOL, METHYLPARABEN, BISABOLOL, ALLANTOIN, PROPYLPARABEN, DISODIUM EDTA, SPIRULINA PLATENSIS EXTRACT, SODIUM HYALURONATE.

Directions

Apply liberaaly 15 minutes before sun exposure.

Children under 6 months; Ask a doctor.

When using this product

keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Do not inhale or ingest.

Avoid contact with broken skin.

Other information

Do not store above 105F.

May discolor some fabrics.

Harmful to wood finishes and plastics.

When using this product

Keep out of eyes,Rinse with water to remove.

Purpose

Sunscreen

Stop use and ask a doctor

if rash occurs.

Do not use

on danaged or broken skin.

Other information

Protect the product in this container from excessive heat and direct sun.

For sunscreen use

Apply to all skin exposed to the sun

Limit time in the sun,especially from 10 a.m.-2 p.m.

Wear long-s;eeved shirts,pants,hats,and sunglasses.

Warnings

Warnings

For external use only

DOSAGE & ADMINISTRATION SECTION

Emulsion，Apply generously 15 minutes before sun exposure

Reapply at least every 2 hours

Keep out of reach of children.

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

Packaging

Packaging

INGREDIENTS AND APPEARANCE

SUN SCREENLOTION SPF30  01
octinoxate,avobenzone,oxybenzone,titanium dioxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54860-417
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	8.5 g  in 100 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	3 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCYRRHIZA URALENSIS (UNII: 42B5YD8F0K)
CAPRYLIC/CAPRIC/PALMITIC/STEARIC TRIGLYCERIDE (UNII: ZF29F7IK5I)
PEG-100 STEARATE (UNII: YD01N1999R)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
ENZACAMENE (UNII: 8I3XWY40L9)
VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
CETEARETH-25 (UNII: 8FA93U5T67)
.ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
XANTHAN GUM (UNII: TTV12P4NEE)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54860-417-01	45 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/19/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	10/19/2023

Labeler - Shenzhen Lantern Scicence Co.,Ltd. (421222423)

Registrant - LANTERN HEALTH&BEAUTY LAB INC. (086860340)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Lantern Science Co.,Ltd.		421222423	manufacture(54860-417)