NIGHTLY FACE TREATMENT - DIMETHICONE- dimethicone cream

NIGHTLY FACE TREATMENT - DIMETHICONE by

Drug Labeling and Warnings

NIGHTLY FACE TREATMENT - DIMETHICONE by is a Otc medication manufactured, distributed, or labeled by ARG LABORATORIES INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

DIMETHICONE 1.5%

PURPOSE

SKIN PROTECTANT

USES

Temporarily protects and helps relieve chapped or cracked skin.
Helps protect from the drying effect of wind and cold weather.

WARNINGS

For external use only

When using this product
Do not get into eyes

Stop use and ask a doctor if
Condition worsens

Symptoms last more than 7 days or clear up and occur again within a few days

Do not use

On deep puncture wounds

Animal bites

Serious burns

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.

DIRECTIONS

Apply as needed. After cleansing skin thoroughly, apply four (+/-) pumps to face and neck. Apply to slightly damp skin for optimal absorption. Rinse skin in the morning following usage.

INACTIVE INGREDIENTS

WATER (AQUA), ALOE BARBADENSIS LEAF JUICE, HYDROLYZED EGG SHELL MEMBRANE, NERIUM OLEANDER LEAF EXTRACT, NIACINAMIDE GLYCERIN, PROPANEDIOL,BUTYLENE GLYCOL, GLYCERYL STEARATE, Hydroxyethylacrylate/Sodium
Acryloyldimethyltaurate Copolymer, Hydrogenated Polydecene, Cocos Nucifera (Coconut) Oil, Caprylic/Capric Triglyceride, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, SQUALANE, Cetearyl Olivate, Sorbitan Olivate, C12-15 Alkyl Benzoate, Stearic Acid, LEUCONOSTOC/RADISH ROOT FERMENT, Butyrospermum Parkii (Shea) Butter, Theobroma Cacao (Cocoa) Seed Butter, Polysorbate 80, CAPRYLYL GLYCOL, SALVIA HISPANICA (CHIA) SEED OIL, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT, Sodium Lactate, Tocopheryl Acetate, Xanthan Gum, Cymbopogon Schoenanthus Extract, Disodium EDTA, Acetyl Hexapeptide-30, Alteromonas Ferment Extract, Arginine, Caramel, POTASSIUM SORBATE, GLYCERYL CAPRYLATE, PHENYLPROPANOL, Limonene, Citral, Hydroxycitronellal, Linalool.

QUESTIONS?

1-(844)-599-7787  M-F (9 AM TO 5 PM CST)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NIGHTLY FACE TREATMENT - DIMETHICONE 
dimethicone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71593-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	1.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
EGG SHELL MEMBRANE (UNII: N7QBR4212V)
NERIUM OLEANDER LEAF (UNII: 7KV510R6H6)
NIACINAMIDE (UNII: 25X51I8RD4)
GLYCERIN (UNII: PDC6A3C0OX)
PROPANEDIOL (UNII: 5965N8W85T)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
COCONUT OIL (UNII: Q9L0O73W7L)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
SUNFLOWER OIL (UNII: 3W1JG795YI)
SQUALANE (UNII: GW89575KF9)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
SORBITAN OLIVATE (UNII: MDL271E3GR)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
STEARIC ACID (UNII: 4ELV7Z65AP)
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
SHEA BUTTER (UNII: K49155WL9Y)
COCOA BUTTER (UNII: 512OYT1CRR)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SALVIA HISPANICA SEED (UNII: NU0OLX06F8)
ROSEMARY (UNII: IJ67X351P9)
SODIUM LACTATE (UNII: TU7HW0W0QT)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
XANTHAN GUM (UNII: TTV12P4NEE)
CYMBOPOGON SCHOENANTHUS WHOLE (UNII: RJJ0F54DE8)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ACETYL HEXAPEPTIDE-49 (UNII: 4055X1S509)
ALTEROMONAS MACLEODII (UNII: BPX036043D)
ARGININE (UNII: 94ZLA3W45F)
CARAMEL (UNII: T9D99G2B1R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
PHENYLPROPANOL (UNII: 0F897O3O4M)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
CITRAL (UNII: T7EU0O9VPP)
HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
LINALOOL, (+)- (UNII: F4VNO44C09)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71593-101-51	1 in 1 BOX	12/06/2017
1	NDC: 71593-101-11	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	12/06/2017

Labeler - ARG LABS (049099177)