AROMA MATTE DAY SUNSCREEN SPF-30- octinoxate, octisalate, zinc oxide cream

AROMA MATTE DAY by

Drug Labeling and Warnings

AROMA MATTE DAY by is a Otc medication manufactured, distributed, or labeled by CONTROL CORRECTIVE SKINCARE INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

OCTINOXATE (6.9%)

OCTISALATE (3.0%)

ZINC OXIDE (4.0%)

PURPOSE

SUNSCREEN

USE

A MULTI-PURPOSE SUNSCREEN AND FACIAL MOISTURIZER. OFFERS BROAD SPECTRUM UVA & UVB PROTECTION WITHOUT LEAVING A GREASY FILM. HELPS PREVENT AGAINST TANNING AND BURNING. CONTAINS ALOE VERA AND ANTIOXIDANTS TO HELP SOOTHE AND BALANCE THE SKIN. MAY BE USED AS A FACIAL MOISTURIZER TO HELP FIGHT THE SIGNS OF AGING WHICH INCLUDES WRNKLING, DRYNESS, PIGMENTATION AND REDNESS.

WARNING

FOR EXTERNAL USE ONLY. WHEN USING THIS PRODUCT, AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER. DISCONTINUE USE AND ASK A DOCTOR IF IRRITATION OR RASH DEVELOPS.

DIRECTIONS

APPLY TO CLEAN SKIN AT LEAST 15 MINUTES PRIOR TO SUN EXPOSURE. MAY BE USED AS OFTEN AS DESIRED. PENETRATES QUICKLY LEAVING A MATTE FINISH. SAFE FOR SENSITIVE SKIN.

OTHER SAFETY INFORMATION

SUN ALERT: LIMITING SUN EXPOSURE, WEARING PROTECTIVE CLOTHING, AND USING SUNSCREEN MAY REDUCE THE RISK OF SKIN AGING, SKIN CANCER, AND OTHER HARMFUL EFFECTS OF THE SUN.

INACTIVE INGREDIENTS

WATER, ALOE BARBADENSIS LEAF, GLYCERIN, PROPYLENE GLYCOL, ISOPROPYL PALMITATE, CAPRYLIC/CAPRIC TRIGLYCERIDES, CYCLOPENTASILOXANE, CETEARYL ALCOHOL, CETEARETH-20, VP/EICOSENE COPOLYMER, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, SQUALANE, POLYSORBATE 60, CYCLOTETRASILOXANE, PHENOXYETHANOL, FRAGRANCE, BUTYROSPERMUM PARKII SHEA BUTTER, PERSEA GRATISSIMA OIL, TOCOPHERYL ACETATE, DISODIUM EDTA, TRIETHOXYCAPRYLYLSILANE, ASPALATHUS LINEARIS LEAF EXTRACT, CAMELLIA OLEIFERA LEAF EXTRACT, DIPROPYLENE GLYCOL, BOSWELLIA SERRATA GUM, CITRIC ACID, METHYLISOTHIAZOLINONE, SODIUM ASCORBYL PHOSPHATE, CHOLECALCIFEROL

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.

QUESTIONS OR COMMENTS

WWW.CONTROLCORRECTIVE.COM

TOLL FREE 1-866-290-4290  MADE IN USA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AROMA MATTE DAY   SUNSCREEN SPF-30
octinoxate, octisalate, zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70764-208
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	6.9 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	3 g  in 100 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
SQUALANE (UNII: GW89575KF9)
POLYSORBATE 60 (UNII: CAL22UVI4M)
SHEA BUTTER (UNII: K49155WL9Y)
AVOCADO OIL (UNII: 6VNO72PFC1)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
ASPALATHUS LINEARIS LEAF (UNII: H7UGK1GJCU)
CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
CYCLOMETHICONE 4 (UNII: CZ227117JE)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
EDETATE DISODIUM (UNII: 7FLD91C86K)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
CHOLECALCIFEROL (UNII: 1C6V77QF41)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70764-208-52	1 in 1 BOX	09/11/2018
1		74 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	M020	09/11/2018

Labeler - CONTROL CORRECTIVE SKINCARE INC (023999357)