PERRICONE MD NEUROPEPTIDE RESTORATIVE NECK AND CHEST THERAPY BROAD SPECTRUM SPF 25- titanium dioxide cream

Perricone MD Neuropeptide Restorative Neck and Chest Therapy Broad Spectrum SPF 25 by

Drug Labeling and Warnings

Perricone MD Neuropeptide Restorative Neck and Chest Therapy Broad Spectrum SPF 25 by is a Otc medication manufactured, distributed, or labeled by THG Beauty USA LLC, Dimensional Merchandising Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Titanium Dioxide 4.2%

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 skin 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

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

DOSAGE & ADMINISTRATION

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.

INACTIVE INGREDIENT

Water/Aqua/Eau, Dimethicone, Cyclopentasiloxane, Glycerin, Ethylhexyl Methoxycrylene, Niacinamide, Pentylene Glycol, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polyester-8, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Benzyl Alcohol, Aluminum Hydroxide, Stearic Acid, Isohexadecane, Diethylhexyl Syringylidenemalonate, Hydrogenated Lecithin, Polysilicone-11, Mannitol, Bisabolol, Polysorbate 60, Tetrahexyldecyl Ascorbate, Sorbitan Isostearate, Phenoxyethanol, Caprylic/Capric Triglyceride, Potassium Sorbate, Sodium Benzoate, Xanthan Gum, Hydrogenated Phosphatidylcholine, Thioctic Acid, Acetyl Tetrapeptide-9

QUESTIONS

1-888-823-7837

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PERRICONE MD NEUROPEPTIDE RESTORATIVE NECK AND CHEST THERAPY BROAD SPECTRUM SPF 25 
titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84448-447
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	4.2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
XANTHAN GUM (UNII: TTV12P4NEE)
HYDROGENATED SOYBEAN PHOSPHATIDYLCHOLINE (UNII: QHQ97HF0PY)
THIOCTIC ACID (UNII: 73Y7P0K73Y)
POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
MANNITOL (UNII: 3OWL53L36A)
DIMETHICONE (UNII: 92RU3N3Y1O)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
POLYSORBATE 60 (UNII: CAL22UVI4M)
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
ISOHEXADECANE (UNII: 918X1OUF1E)
STEARIC ACID (UNII: 4ELV7Z65AP)
GLYCERIN (UNII: PDC6A3C0OX)
NIACINAMIDE (UNII: 25X51I8RD4)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
BENZYL ALCOHOL (UNII: LKG8494WBH)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LEVOMENOL (UNII: 24WE03BX2T)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
ACETYL TETRAPEPTIDE-9 (UNII: VMO8OOD3V0)
POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Product Characteristics
Color	yellow	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84448-447-18	1 in 1 CARTON	01/29/2018
1		118 mL in 1 JAR; Type 0: Not a Combination Product
2	NDC: 84448-447-59	1 in 1 CARTON	01/29/2018
2		59 mL in 1 JAR; 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	01/29/2018

Labeler - THG Beauty USA LLC (015792160)

Establishment
Name	Address	ID/FEI	Business Operations
Dimensional Merchandising Inc		076693183	manufacture(84448-447)