DAILY PREVENTION SHEER MATTE MOISTURIZER SPF30- homosalate and octisalate and zinc oxide cream

Daily Prevention Sheer Matte Moisturizer SPF30 by

Drug Labeling and Warnings

Daily Prevention Sheer Matte Moisturizer SPF30 by is a Otc medication manufactured, distributed, or labeled by Allure Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients

Homosalate 5.0%

Octisalate 5.0%

Zinc Oxide 9.3%

PURPOSE

Purpose: Sunscreen

INDICATIONS & USAGE

Uses 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

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 right away.

DOSAGE & ADMINISTRATION

Directions apply generously 15 minutes before sun exposure children under 6 months of age: Ask a doctor reapply: after 40 minutes of swimming or sweating immediately after towel drying at least every 2 hours 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

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

INACTIVE INGREDIENT

Inactive ingredients: Aqua/water/Eau, Cyclopentasiloxane, Polyhydroxystearic Acid, Dimethicone, Coconut Alkanes, Stearic Acid, Lecithin, Aloe Barbadensis Leaf Juice, Isohexadecane, lsododecane, Magnesium Sulfate, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Triethoxysilylethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Polysillcone-11, Coco-Caprylate/Caprate, Dimethicone/PEG-10/15 Crosspolymer, Dipropylene Glycol, Sodium Citrate, Tocopherol, Cetearyl Olivate, Sorbitan Olivate, Sodium Hyaluronate, Phenoxyethanol, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Squalane, Polysorbate 60, Sorbitan Isostearate, Caprylyl Glycol, Ethylhexylycerin, Hexylene Glycol, Phosphatidylcholine, Mannitol, Glycerin, Methylpropanediol, Caprylic/Capric Triglyceride, Ectoine, Palmitic Acid, Haematococcus Pluvialis Extract, Tetrahexyldecyl Ascorbate, Panthenol, Phenylpropanol, Vanilla Planifolia Fruit Extract, Silica, Dimethicone/Vinyl Dimethicone Crosspolymer, Acetyl Zingerone, Camellia Sinensis Leaf Extract, Sodium Benzoate, Potassium Sorbate, Octyldodecanol, Sorbitan Oleate, CI 77491, CI 77492

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DAILY PREVENTION SHEER MATTE MOISTURIZER SPF30 
homosalate and octisalate and zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4253
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	5 g  in 100 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	9.3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)
MANNITOL (UNII: 3OWL53L36A)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
OCTYLDODECANOL (UNII: 461N1O614Y)
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
WATER (UNII: 059QF0KO0R)
TRIETHOXYSILYLETHYL POLYDIMETHYLSILOXYETHYL HEXYL DIMETHICONE (UNII: X75PL53TZJ)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
METHYLPROPANEDIOL (UNII: N8F53B3R4R)
ECTOINE (UNII: 7GXZ3858RY)
PALMITIC ACID (UNII: 2V16EO95H1)
PANTHENOL (UNII: WV9CM0O67Z)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
ISODODECANE (UNII: A8289P68Y2)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
TOCOPHEROL (UNII: R0ZB2556P8)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
SORBITAN OLIVATE (UNII: MDL271E3GR)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
PHOSPHATIDYLCHOLINE TRANSLOCATOR ABCB4 (UNII: 9EI49ZU76O)
HAEMATOCOCCUS PLUVIALIS (UNII: 31T0FF0472)
VANILLA (UNII: Q74T35078H)
FERRIC OXIDE RED (UNII: 1K09F3G675)
SQUALANE (UNII: GW89575KF9)
ACETYL ZINGERONE (UNII: V9D92S9YE5)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ISOHEXADECANE (UNII: 918X1OUF1E)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
POLYSORBATE 60 (UNII: CAL22UVI4M)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
DIMETHICONE (UNII: 92RU3N3Y1O)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
COCONUT ALKANES (UNII: 1E5KJY107T)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
PHENYLPROPANOL (UNII: 0F897O3O4M)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
STEARIC ACID (UNII: 4ELV7Z65AP)
DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4253-1	7 g in 1 TUBE; Type 0: Not a Combination Product	03/15/2024
2	NDC: 62742-4253-2	28 g in 1 TUBE; Type 0: Not a Combination Product	03/15/2024
3	NDC: 62742-4253-4	1 in 1 CARTON	03/15/2024
3	NDC: 62742-4253-3	73 g in 1 TUBE; Type 0: Not a Combination Product
4	NDC: 62742-4253-5	142 g in 1 TUBE; Type 0: Not a Combination Product	03/15/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	03/15/2024

Labeler - Allure Labs (926831603)

Registrant - Allure Labs (926831603)

Establishment
Name	Address	ID/FEI	Business Operations
Allure Labs		926831603	manufacture(62742-4253)