SILK SPF FACIAL SUNSCREEN FLUID HYBRID BROAD SPECTRUM SPF 30 UVA/UVB- zinc oxide and homosalate cream

silk SPF facial sunscreen fluid hybrid broad spectrum SPF 30 UVA/UVB by

Drug Labeling and Warnings

silk SPF facial sunscreen fluid hybrid broad spectrum SPF 30 UVA/UVB by is a Otc medication manufactured, distributed, or labeled by OneKind.25. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients

Zinc Oxide 10.5%

Homosalate 10%

PURPOSE

Purpose

Sunscreen

INDICATIONS & USAGE

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

Warnings
For external use only.

DO NOT USE

Do not use on damaged or broken skin.

WHEN USING

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

STOP USE

Stop use and ask a doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Directions
Apply generously 15 minutes before sun
exposure. Reapply at least every 2 hours.
Use a water-resistant sunscreen if
swimming or sweating.

OTHER SAFETY INFORMATION

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. Children under 6
months of age: ask a doctor.

INACTIVE INGREDIENT

Inactive Ingredients
water/aqua/eau, caprylic/capric
triglyceride, glyceryl stearate se, coconut
alkanes, glycerin, coco-caprylate/caprate,
decyl glucoside, oryza sativa (rice) starch,
musa sapientum (banana) flower extract,
polyhydroxystearic acid, polyglyceryl-3
polyricinoleate, isostearic acid, lecithin,
xanthan gum, hydroxyethylcellulose,
caprylyl glycol, caprylhydroxamic acid,
sodium benzoate, citric acid, disodium
phosphate, sodium phosphate.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SILK SPF FACIAL SUNSCREEN FLUID HYBRID BROAD SPECTRUM SPF 30 UVA/UVB 
zinc oxide and homosalate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79356-202
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	10.5 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
MUSA X PARADISIACA FLOWER (UNII: DG5B0M0NGY)
WATER (UNII: 059QF0KO0R)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
SODIUM PHOSPHATE (UNII: SE337SVY37)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
COCONUT ALKANES (UNII: 1E5KJY107T)
GLYCERIN (UNII: PDC6A3C0OX)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
ISOSTEARIC ACID (UNII: X33R8U0062)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
XANTHAN GUM (UNII: TTV12P4NEE)
SODIUM BENZOATE (UNII: OJ245FE5EU)
STARCH, RICE (UNII: 4DGK8B7I3S)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79356-202-02	1 in 1 CARTON	02/01/2022
1	NDC: 79356-202-01	48 g 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 Drug	M020	02/01/2022

Labeler - OneKind.25 (080286020)