Drug Facts

Active ingredient(s)	Purpose
Titanium dioxide 11.7%	Sunscreen
Zinc oxide 20%	Sunscreen

Uses

helps prevent sunburn
if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs

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

For sunscreen use:

apply liberally 15 minutes before sun exposure
children under 6 months: ask a doctor
use a water resistant sunscreen if swimming or sweating
reapply at least every 2 hours
Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m. – 2 p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses

Protect this product from excessive heat and direct sun

bismuth oxychloride, mica, iron oxides.

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bareMinerals ®

ORIGINAL FOUNDATION
Broad Spectrum SPF 15

GOLDEN TAN 20

net wt. 8 g / 0.28 oz.

61276

BAREMINERALS ORIGINAL FOUNDATION BROAD SPECTRUM SPF 15 GOLDEN TAN 20
titanium dioxide and zinc oxide powder

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	936 mg in 8 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	1600 mg in 8 g

Ingredient Name	Strength
Inactive Ingredients
MICA (UNII: V8A1AW0880)
FERRIC OXIDE RED (UNII: 1K09F3G675)
BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:98132-019-08	8 g in 1 JAR; Type 0: Not a Combination Product	08/01/2021
2	NDC:98132-019-02	2 g in 1 JAR; Type 0: Not a Combination Product	08/01/2021
3	NDC:98132-019-75	0.75 g in 1 JAR; Type 0: Not a Combination Product	08/01/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	08/01/2021

Labeler - Orveon Global US LLC (118344494)