Label: MINERAL WEAR AIRBRUSHING PRESSED POWDER- titanium dioxide, zinc oxide powder
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Contains inactivated NDC Code(s)
NDC Code(s): 31645-214-01 - Packager: Physicians Formula, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated September 28, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
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Directions
apply liberally 15 minutes before sun exposure
use a water resistant sunscreen if swimming or sweating
reapply at least every 2 hours
children under 6 months of age: Ask a doctor
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 value 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
- Other information
- Inactive ingredients
- Questions or comments?
- Mineral Wear Airbrushing Pressed Powder
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INGREDIENTS AND APPEARANCE
MINERAL WEAR AIRBRUSHING PRESSED POWDER
titanium dioxide, zinc oxide powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:31645-214 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 15 g in 100 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 10 g in 100 g Inactive Ingredients Ingredient Name Strength MICA (UNII: V8A1AW0880) LAUROYL LYSINE (UNII: 113171Q70B) PHENOXYETHANOL (UNII: HIE492ZZ3T) HEXYLENE GLYCOL (UNII: KEH0A3F75J) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) ZINC STEARATE (UNII: H92E6QA4FV) BORON NITRIDE (UNII: 2U4T60A6YD) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) O-CYMEN-5-OL (UNII: H41B6Q1I9L) FERROSOFERRIC OXIDE (UNII: XM0M87F357) CALCIUM ALUMINUM BOROSILICATE (UNII: 3JRB8A35M0) GINKGO BILOBA LEAF OIL (UNII: Y5967KO1JH) TRICAPRYLIN (UNII: 6P92858988) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) PANAX GINSENG LEAF (UNII: F055A23N6X) SAFFLOWER OIL (UNII: 65UEH262IS) ASCORBYL PALMITATE (UNII: QN83US2B0N) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:31645-214-01 7.5 g in 1 CONTAINER; Type 0: Not a Combination Product 01/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 01/01/2019 Labeler - Physicians Formula, Inc. (021261805)
