ULTRA VIOLETTE SEQUIN SUPREME SPF 50- octocrylene, homosalate, octisalate, avobenzone lotion

Ultra Violette Sequin Supreme SPF 50 by

Drug Labeling and Warnings

Ultra Violette Sequin Supreme SPF 50 by is a Otc medication manufactured, distributed, or labeled by Grace and Fire USA Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

AVOBENZONE 3.0%

HOMOSALATE 7.0%

OCTISALATE 5.0%

OCTOCRYLENE 8.0%

Purpose

SUNSCREEN

USE

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 SECTION

For External Use Only

Do not use

on damaged or broken skin

Keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

rash occurs

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

Directions

Directions for Sunscreen Use

• apply liberally and evenly 15 minutes before sun exposure
• reapply at least every 2 hours
• use a water resistant sunscreen if swimming or sweating
• 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, especally from 10 a.m. - 2 p.m.
• wear long-sleeved shirts, pants, hats, and sunglasses
• children under 6 months of age, Ask a doctor

Inactive Ingredients

Water, Alcohol Denat., Butylene Glycol, Copernicia Cerifera (Carnauba) Wax, Glycerin, Diisopropyl Adipate, Mica, Cetearyl Alcohol, Caprylyl Methicone, Isododecane, Dimethicone, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Ceteareth-20, Nylon-6/12, Oryza Sativa (Rice) Bran Wax, Polysorbate 60, Saccharide Isomerate, Squalane, Carnosine, Tocopheryl Acetate, Terminalia Ferdinandiana (Kakadu Plum) Fruit Extract, Silica, PEG-40 Stearate, Citric Acid, Glyceryl Caprylate, Fragrance, Disodium EDTA, Pentylene Glycol, Caprylhydroxamic Acid, Triethanolamine, Lactic Acid, Sorbitan Isostearate, Sodium Citrate, Titanium Dioxide (CI 77891), Iron Oxides (CI 77492), Iron Oxides (CI 77491), Iron Oxides (CI 77499).

STORAGE AND HANDLING

Other Information

Other information protect the product in this container from excessive heat and direct sun

PRINCIPLE DISPLAY PANEL.

ULTRA

VIOLETTE

SEQUIN SUPREME SPF 50

GLOW -BOOSTING

PRIMING SUNSCREEN

UV

FOR A DEWY

HYDRATED FINISH

Broad Spectrum SPF 50

Sunscreen PA++++

50ml 1.7fl.oz

INGREDIENTS AND APPEARANCE

ULTRA VIOLETTE SEQUIN SUPREME SPF 50 
octocrylene, homosalate, octisalate, avobenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84803-107
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	70 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	80 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
HYDRATED SILICA (UNII: Y6O7T4G8P9)	0.25 mg  in 1 mL
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)	0.021 mg  in 1 mL
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)	1.5 mg  in 1 mL
T-BUTYL ALCOHOL (UNII: MD83SFE959)	0.005 mg  in 1 mL
POLYSORBATE 60 (UNII: CAL22UVI4M)	0.07 mg  in 1 mL
PENTYLENE GLYCOL (UNII: 50C1307PZG)	0.075 mg  in 1 mL
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)	0.05 mg  in 1 mL
CETEARETH-20 (UNII: YRC528SWUY)	0.5 mg  in 1 mL
COPERNICIA CERIFERA (CARNAUBA) WAX (UNII: R12CBM0EIZ)	1.9 mg  in 1 mL
PEG-40 STEARATE (UNII: ECU18C66Q7)	0.25 mg  in 1 mL
CI 77492 (UNII: EX438O2MRT)	0.03 mg  in 1 mL
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)	0.1 mg  in 1 mL
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)	2 mg  in 1 mL
CARNOSINE (UNII: 8HO6PVN24W)	0.03 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)	0.58 mg  in 1 mL
ORYZA SATIVA (RICE) BRAN (UNII: R60QEP13IC)	0.1 mg  in 1 mL
WATER (UNII: 059QF0KO0R)	19.25 mg  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	1.77 mg  in 1 mL
DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)	1.5 mg  in 1 mL
KAKADU PLUM (UNII: 0ZQ1D2FDLI)	0.02 mg  in 1 mL
CITRIC ACID (UNII: 2968PHW8QP)	0.003 mg  in 1 mL
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)	0.51 mg  in 1 mL
ALCOHOL (UNII: 3K9958V90M)	2.49 mg  in 1 mL
CAPRYLYL METHICONE (UNII: Q95M2P1KJL)	1 mg  in 1 mL
ISODODECANE (UNII: A8289P68Y2)	1 mg  in 1 mL
DIMETHICONE (UNII: 92RU3N3Y1O)	0.75 mg  in 1 mL
NYLON 612 (18000 MW) (UNII: X288170XH1)	0.5 mg  in 1 mL
LACTIC ACID (UNII: 33X04XA5AT)	0.025 mg  in 1 mL
CI 77491 (UNII: 1K09F3G675)	0.008 mg  in 1 mL
CI 77499 (UNII: XM0M87F357)	0.0035 mg  in 1 mL
TRIETHANOLAMINE (UNII: 9O3K93S3TK)	0.025 mg  in 1 mL
CETEARYL ALCOHOL (UNII: 2DMT128M1S)	1 mg  in 1 mL
MICA (UNII: V8A1AW0880)	1.42 mg  in 1 mL
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)	0.375 mg  in 1 mL
SQUALANE (UNII: GW89575KF9)	0.35 mg  in 1 mL
SACCHARIDE ISOMERATE (UNII: W8K377W98I)	0.31 mg  in 1 mL
FRAGRANCE 13576 (UNII: 5EM498GW35)	0.075 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84803-107-50	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/01/2025
2	NDC: 84803-107-15	15 mL in 1 TUBE; Type 0: Not a Combination Product	11/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/01/2025

Labeler - Grace and Fire USA Inc. (119357605)