PERRICONE MD HYPOALLERGENIC CLEAN CORRECTION ULTRA-LIGHTWEIGHT CALMING SPF 35 VEIL- zinc oxide cream

Perricone MD Hypoallergenic Clean Correction Ultra-Lightweight Calming SPF 35 Veil by

Drug Labeling and Warnings

Perricone MD Hypoallergenic Clean Correction Ultra-Lightweight Calming SPF 35 Veil by is a Otc medication manufactured, distributed, or labeled by THG Beauty USA LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Zinc Oxide 15.45%

PURPOSE

Sunscreen

INDICATIONS & USAGE

Helps prevent sunburn

if used as directed with other sun protection measures (see ​directions)​, decreases the risk of skin cancer and early signs of aging caused by the sun.

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

If product is swallowed, get medical help or contact a Poison Control Centre right away.

DOSAGE & ADMINISTRATION

Directions
For Sunscreen Use:
■ Apply liberally 15 minutes before sun exposure.
■ Use a water resistant sunscreen if swimming or sweating.
■ Reapply at least every 2 hours.
■ Not for use on children.
■ 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 SAFETY INFORMATION

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

INACTIVE INGREDIENT

Water/Aqua/Eau, Isododecane, Caprylic/Capric Triglyceride, Coco-Caprylate/Caprate, Acrylates Copolymer, C12-15 Alkyl Benzoate, Butyloctyl Salicylate, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Glycerin, Propanediol, Cannabis Sativa Seed Oil, Sodium Chloride, Polyhydroxystearic Acid, Triheptanoin, Stearalkonium Hectorite, Calendula Officinalis Flower Extract, Stearoyl Glutamic Acid, Hydroxyacetophenone, Xanthan Gum, C9-12 Alkane, Dilinoleic Acid/Butanediol Copolymer, Propylene Carbonate, Sodium Benzoate, Dipotassium Glycyrrhizate, Vaccinium Vitis-Idaea Fruit Extract, Potassium Sorbate, Bisabolol, Oryza Sativa (Rice) Bran Extract, Castor Oil/IPDI Copolymer, Octyldodecanol, Rosmarinus Officinalis (Rosemary) Leaf Extract, Citric Acid, Gluconolactone, Helianthus Annuus (Sunflower) Extract, Tocopherol, Calcium Gluconate.

QUESTIONS

1-888-823-7837

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PERRICONE MD HYPOALLERGENIC CLEAN CORRECTION ULTRA-LIGHTWEIGHT CALMING SPF 35 VEIL 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84448-402
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	15.45 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
TRIHEPTANOIN (UNII: 2P6O7CFW5K)
CASTOR OIL/IPDI COPOLYMER (UNII: GSA2TXZ34G)
CITRIC ACID (UNII: 2968PHW8QP)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
DILINOLEIC ACID/BUTANEDIOL COPOLYMER (UNII: 1F2S8T535O)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
CALCIUM GLUCONATE (UNII: SQE6VB453K)
ISODODECANE (UNII: A8289P68Y2)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
STEAROYL GLUTAMIC ACID (UNII: 4R4O71786G)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
OCTYLDODECANOL (UNII: 461N1O614Y)
LINGONBERRY (UNII: 0UNK9RZQ7X)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
BISABOLOL (UNII: 24WE03BX2T)
ROSEMARY (UNII: IJ67X351P9)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
GLYCERIN (UNII: PDC6A3C0OX)
DIPOTASSIUM GLYCYRRHIZATE (UNII: CA2Y0FE3FX)
PROPANEDIOL (UNII: 5965N8W85T)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)
TOCOPHEROL (UNII: R0ZB2556P8)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)
ORYZA SATIVA (RICE) BRAN (UNII: R60QEP13IC)
C9-12 ALKANE (UNII: 7J5R5W72QM)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84448-402-15	1 in 1 CARTON	10/04/2022
1		15 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 84448-402-50	1 in 1 CARTON	10/04/2022
2		50 mL 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	10/04/2022

Labeler - THG Beauty USA LLC (015792160)