CLEAR CLEAR ZINC SOLAR PROTECTION SPF 30- zinc oxide cream

Clear Clear Zinc Solar Protection SPF 30 by

Drug Labeling and Warnings

Clear Clear Zinc Solar Protection SPF 30 by is a Otc medication manufactured, distributed, or labeled by Allure Labs, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Zinc Oxide: 17%

PURPOSE

Purpose:

Suncreen

INDICATIONS & USAGE

Uses: Help prevent sunburn

WARNINGS

Warnings: For external use only

DO NOT USE

Do not use on damged or broken skin.

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Directions: Massage into skin with fingertips and reapply as needed. Avoid eye area while applying.

INACTIVE INGREDIENT

Other Ingredients: Water (Aqua), Cyclopentasiloxane, Dimethicone/PEG10/15 Crosspolymer, Dimethicone/Vinyl Dimethicone Crossploymer, Polyglyceryl-3 polydimethylsiloxyethyl Dimethicone, Cyclomethicone, PEG/PPG-18/18 Dimethicone, Hexyl Triethoxysilylethyl Polydimethylsiloxyethyl Dimethicone, C12-15 Alkyl Benzoate, Polyisobutene, Isododecane, Phenoxyethanol, Sodium Hyaluronate, Caprylyl Glycol, Tocopheryl Acetate, Ethylhexylglycerin, Hexylene Glycol, Mica, Aloe Barbadensis Leaf extract, Camellia Sinensis Leaf Extract, Olea Europaea (Olive) Leaf Extract, Silica

PRINCIPAL DISPLAY PANEL

Physicians' Aesthetic Research, Inc. Distr.

San Clemente, CA 92672 . Made in U.S.A. www.lucrece.com

INGREDIENTS AND APPEARANCE

CLEAR CLEAR ZINC SOLAR PROTECTION SPF 30 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4109
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	170 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)
CYCLOMETHICONE (UNII: NMQ347994Z)
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)
ISODODECANE (UNII: A8289P68Y2)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
MICA (UNII: V8A1AW0880)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)
OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4109-1	71 g in 1 TUBE; Type 0: Not a Combination Product	12/04/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	12/04/2017

Labeler - Allure Labs, Inc (926831603)

Registrant - Allure Labs, Inc (926831603)

Establishment
Name	Address	ID/FEI	Business Operations
Allure Labs, Inc		926831603	manufacture(62742-4109)