SILK MINERAL SPF 50 SUNSCREEN FACE- zinc oxide lotion

Silk Mineral SPF 50 Sunscreen Face by

Drug Labeling and Warnings

Silk Mineral SPF 50 Sunscreen Face by is a Otc medication manufactured, distributed, or labeled by Baxter Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient Purpose

Zinc Oxide20%....Sunscreen

PURPOSE

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.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If product is swallowed, get medical help or contact a poison control center right awa.

INDICATIONS & USAGE

Stop use and ask a doctor if rash occurs.

WARNINGS

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.

DOSAGE & ADMINISTRATION

Directions

Apply liberally 15 minutes before sun exposure

Reapply at least every 2 hours

INACTIVE INGREDIENT

Ingredients

Aqua/Water/Eau, Coco-Caprylate/Caprate, Isohexadecane, Caprylic/Capric Triglyceride, Coco-Caprylate, Polyglyceryl-2 Dipolyhydroxystearate, Isoamyl Laurate, Pentylene Glycol, Isododecane, Polyglyceryl-3 Polyricinoleate, Polyglyceryl-3 Diisostearate, Sorbitan Olivate, Magnesium Sulfate, Polyhydroxystearic Acid, Glycerin, Pongamia Pinnata Seed Extract, Terminalia Ferdinandiana Fruit Extract, Isostearic Acid, Disteardimonium Hectorite, Hydroxyacetophenone, Propylene Carbonate

PRINCIPAL DISPLAY PANEL

Standard Procedure

Silk Mineral SPF 50 Sunscreen Face Lotion

1.7 fl oz 50 mL

INGREDIENTS AND APPEARANCE

SILK MINERAL SPF 50 SUNSCREEN FACE 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70157-026
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	20 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PENTYLENE GLYCOL (UNII: 50C1307PZG)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
GLYCERIN (UNII: PDC6A3C0OX)
KAKADU PLUM (UNII: 0ZQ1D2FDLI)
WATER (UNII: 059QF0KO0R)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
COCO-CAPRYLATE (UNII: 4828G836N6)
POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
ISODODECANE (UNII: A8289P68Y2)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
PONGAMIA PINNATA SEED (UNII: C2BRV53B1V)
ISOSTEARIC ACID (UNII: X33R8U0062)
ISOAMYL LAURATE (UNII: M1SLX00M3M)
ISOHEXADECANE (UNII: 918X1OUF1E)
SORBITAN OLIVATE (UNII: MDL271E3GR)
MAGNESIUM SULFATE (UNII: DE08037SAB)
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70157-026-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/09/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	05/09/2025

Labeler - Baxter Laboratories (740537709)