MINERAL FOUNDATION SPF 30-5W- zinc oxide and titanium dioxide cream

Mineral Foundation SPF 30-5W by

Drug Labeling and Warnings

Mineral Foundation SPF 30-5W by is a Otc medication manufactured, distributed, or labeled by Allure Labs Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients:

Zinc Oxide - 5.5%

Titanium Dioxide - 4.4%

INDICATIONS & USAGE

Direction: Apply with a foundation brush for flawless coverage. Discontinue use if irritation develpos.

DOSAGE & ADMINISTRATION

Directions: Apply with a foundation brush for flawless coverage. Discontinue use if irritation develops.

PRINCIPAL DISPLAY PANEL

Manufactured for DermaQuest Inc.

Hayward, CA 94544

dermaminerals.com

1272 GK, NL

Made in USA

INGREDIENTS AND APPEARANCE

MINERAL FOUNDATION SPF 30-5W 
zinc oxide and titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4099
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	55 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	44 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
DIMETHICONE (UNII: 92RU3N3Y1O)
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE (UNII: NMQ347994Z)
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
PERFLUNAFENE (UNII: 54A06VV62N)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
SACCHAROMYCES LYSATE (UNII: R85W246Z1C)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E)
MAGNESIUM SILICATE (UNII: 9B9691B2N9)
NYLON-12 (UNII: 446U8J075B)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
SANDALWOOD (UNII: 3641YW25N2)
PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G)
BARLEY (UNII: 5PWM7YLI7R)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
SORBITAN OLIVATE (UNII: MDL271E3GR)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)
STEARIC ACID (UNII: 4ELV7Z65AP)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
HEXYL LAURATE (UNII: 4CG9F9W01Q)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4099-2	1 in 1 CARTON	12/05/2017
1	NDC: 62742-4099-1	29.6 mL 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	11/29/2017

Labeler - Allure Labs Inc. (926831603)