SKIN PERFECTING CC BROAD SPECTRUM SUNSCREEN SPF 48- zinc oxide cream

Skin Perfecting CC Broad Spectrum Sunscreen SPF 48 by

Drug Labeling and Warnings

Skin Perfecting CC Broad Spectrum Sunscreen SPF 48 by is a Otc medication manufactured, distributed, or labeled by Private Label Skin Care. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Zinc Oxide 20.80%

Purpose

​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.

Directions

Apply liberally on a clean dry face, avoiding delicate eye area 15 minutes before sun exposure reapply: after 40 minutes of swimming or sweating immediately after towel drying 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 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

Other information

 protect the product in this container from excessive heat and direct sun

Inactive ingredients

Water/Aqua/Eau, Ethylhexyl Olivate, Coco-Caprylate/Caprate, Polyglyceryl-6 Polyricinoleate, Propanediol, Isododecane, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Jojoba Esters, Titanium Dioxide, Polyglyceryl-10 Dioleate, Sodium Chloride, Dimethicone Crosspolymer, Lentil (Lens Esculenta) Fruit Extract, Apple (Pyrus Malus) Fruit Extract, Watermelon (Citrullus Lanatus) Fruit Extract, 1,2-Hexanediol, Triheptanoin, Squalane, Sodium PCA, Polyhydroxystearic Acid, Dimethicone/Vinyl Dimethicone Crosspolymer, Polyphenylsilsesquioxane, Tocopherol, Polymethylsilsesquioxane/Trimethylsiloxysilicate, Sodium Lactate, Glycerin, Dilinoleic Acid/Butanediol Copolymer, Trihydroxystearin, C9-12 Alkane, Disteardimonium Hectorite, Caprylhydroxamic Acid, Propylene Carbonate, Disodium Stearoyl Glutamate, Silica, Trisodium Ethylenediamine Disuccinate, Castor Oil/IPDI Copolymer, Iron Oxide (CI 77492), Iron Oxide (CI 77491), Iron Oxide (CI 77499)

SPL UNCLASSIFIED SECTION

brand MD

Water Resistant (40 Minutes)
Blue Light Protection

Titanium Dioxide
Iron Oxides
Fruit Extracts

MEDICAL GRADE

SHIELD

Distributed by:
brandMD®
Canoga Park, CA 91304
(818) 534-3180
www.brandMD.com

GREEN LEAF PROGRAM

NOT TESTED ON ANIMALS

RECOMMENDED FOR
 COMBO
 DRY
 NORMAL
SENSITIVE

Packaging

INGREDIENTS AND APPEARANCE

SKIN PERFECTING CC BROAD SPECTRUM SUNSCREEN SPF 48 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72957-014(NDC:39765-056)
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	20.80 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ETHYLHEXYL OLIVATE (UNII: HTC7G3S2PV)
COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)
POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR)
PROPANEDIOL (UNII: 5965N8W85T)
ISODODECANE (UNII: A8289P68Y2)
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)
HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
POLYGLYCERYL-10 DIOLEATE (UNII: 598RES7AXX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
DIMETHICONE CROSSPOLYMER (180000 MPA.S) (UNII: W8CS8KBY2B)
VICIA LENS FRUIT (UNII: ZYZ076G9JH)
APPLE (UNII: B423VGH5S9)
WATERMELON (UNII: 231473QB6R)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
TRIHEPTANOIN (UNII: 2P6O7CFW5K)
SQUALANE (UNII: GW89575KF9)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
PHENYLSILANETRIOL (UNII: DNR46JQ8BT)
TOCOPHEROL (UNII: R0ZB2556P8)
POLYMETHYLSILSESQUIOXANE/TRIMETHYLSILOXYSILICATE (UNII: X2PZH4Y6HT)
SODIUM LACTATE (UNII: TU7HW0W0QT)
GLYCERIN (UNII: PDC6A3C0OX)
DILINOLEIC ACID/BUTANEDIOL COPOLYMER (UNII: 1F2S8T535O)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
C9-12 ALKANE (UNII: 7J5R5W72QM)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
CASTOR OIL/IPDI COPOLYMER (UNII: GSA2TXZ34G)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72957-014-01	57 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/08/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/08/2026

Labeler - Private Label Skin Care (116996962)

Establishment
Name	Address	ID/FEI	Business Operations
Private Label Skin Care		116996962	relabel(72957-014)