PERRICONE MD HYPOALLERGENIC CBD SENSITIVE SKIN THERAPY ULTRA-LIGHTWEIGHT CALMING SPF 35 VEIL- zinc oxide cream

Perricone MD Hypoallergenic CBD Sensitive Skin Therapy Ultra-Lightweight Calming SPF 35 Veil by

Drug Labeling and Warnings

Perricone MD Hypoallergenic CBD Sensitive Skin Therapy 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

• 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 skin aging caused by the sun.

WARNINGS

• For external use only.

• if rash occurs.

• on damaged or broken skin.

• keep out of eyes. Rinse with water to remove

• If swallowed, get medical help or contact a Poison Control Center.

• Not suitable for pregnant or lactating women.

DOSAGE & ADMINISTRATION

• Shake well & apply liberally to face & neck using a gentle upward motion prior to sun exposure.

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, Cannabidiol, 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, Helianthus Annuus (Sunflower) Extract, Citric Acid, Gluconolactone, Rosmarinus Officinalis (Rosemary) Leaf Extract, Tocopherol, Calcium Gluconate

QUESTIONS

• 1-888-823-7837

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PERRICONE MD HYPOALLERGENIC CBD SENSITIVE SKIN THERAPY ULTRA-LIGHTWEIGHT CALMING SPF 35 VEIL 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84448-615
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
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPANEDIOL (UNII: 5965N8W85T)
LEVOMENOL (UNII: 24WE03BX2T)
STEAROYL GLUTAMIC ACID (UNII: 4R4O71786G)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
ROSEMARY (UNII: IJ67X351P9)
WATER (UNII: 059QF0KO0R)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
TOCOPHEROL (UNII: R0ZB2556P8)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
SUNFLOWER OIL (UNII: 3W1JG795YI)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
CANNABIDIOL (UNII: 19GBJ60SN5)
XANTHAN GUM (UNII: TTV12P4NEE)
LINGONBERRY (UNII: 0UNK9RZQ7X)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
C9-12 ALKANE (UNII: 7J5R5W72QM)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ISODODECANE (UNII: A8289P68Y2)
OCTYLDODECANOL (UNII: 461N1O614Y)
RICE BRAN (UNII: R60QEP13IC)
CASTOR OIL/IPDI COPOLYMER (UNII: GSA2TXZ34G)
CALCIUM GLUCONATE (UNII: SQE6VB453K)
DILINOLEIC ACID/BUTANEDIOL COPOLYMER (UNII: 1F2S8T535O)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
TRIHEPTANOIN (UNII: 2P6O7CFW5K)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84448-615-15	1 in 1 CARTON	04/27/2021
1		15 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2	NDC: 84448-615-50	1 in 1 CARTON	04/27/2021
2		50 mL in 1 BOTTLE, PLASTIC; 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	04/27/2021

Labeler - THG Beauty USA LLC (015792160)