LIGHT DAY SUNSCREEN SPF 37- avobenzone, octinoxate, octocrylene lotion

Light Day Sunscreen SPF 37 by

Drug Labeling and Warnings

Light Day Sunscreen SPF 37 by is a Otc medication manufactured, distributed, or labeled by Circadia by Dr Pugliese, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Avobenzone 3.0%
Octinoxate 7.5% 
Octocrylene 2.8%

Purpose

Sunscreen

Uses

helps prevent sunburn

Warnings

For external use only.

Do not use

on damaged or broken skin

When using this product

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

apply liberally to skin 15 minutes before sun exposure.  use a water resistant sunscreen if swimming or sweating. reapply at least every 2 hours. children under 6 months: Ask a doctor. 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 SPF15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m. - 2 p.m. wear long-sleeved shirt, pants, hats, a nd sunglasses.

Inactive ingredients

Water, C12-15 Alkyl Benzoate, Ethylhexyl Methoxycrylene, Glycerin, Silica, VP/Eicosene Copolymer, Glyceryl Stearate, PEG-100 Stearate, Potassium Cetyl Phosphate, Dimethicone, Cyclopentasiloxane, Cyclohexasiloxane, Dimethyl Capramide, Hydrogenated Palm Glycerides,  Polysiloxane-11, Dimethylmethoxy Chromanol, Acrylamide/Sodium Acryloyldimethyltaurate Copolymer, Diaminopropionoyl Tripeptide-33, Caprylyl Glycol, Disodium EDTA, Xanthan Gum, Phenoxyethanol, Hexylene Glycol, Isohexadecane, Polysorbate 80, Prunus Armeniaca Fruit Extract, Aniba Rosaeodora Wood Extract, Citrus Aurantifolia Peel Extract, Citrus Aurantium Dulcis Peel Extract, Vanilla Planifora Fruit Extract, Citrus Grandis Peel Extract, Cocos Nucifera Oil, Vitis Vinifera Fruit Cell Extract, Isomalt, Lecithin, Sodium Benzoate.

Questions?

Call toll-free (800) 630-4710

Package Labeling:(

76458-301-02)

Package Labeling:(

76458-301-08)

INGREDIENTS AND APPEARANCE

LIGHT DAY SUNSCREEN SPF 37 
avobenzone, octinoxate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76458-301
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
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	75 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	28 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
GLYCERIN (UNII: PDC6A3C0OX)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
DIMETHICONE (UNII: 92RU3N3Y1O)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
DIMETHYLMETHOXY CHROMANOL (UNII: XBH432G01F)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
XANTHAN GUM (UNII: TTV12P4NEE)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
ISOHEXADECANE (UNII: 918X1OUF1E)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
ANIBA ROSAEODORA WOOD (UNII: NE01NKA8B2)
LIME PEEL (UNII: 544EQK5Q0W)
ORANGE PEEL (UNII: TI9T76XD44)
VANILLA BEAN (UNII: Q74T35078H)
CITRUS MAXIMA FRUIT RIND (UNII: 5NX3G75CA6)
ISOMALT (UNII: S870P55O2W)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76458-301-02	1 in 1 BOX	02/14/2020
1		59 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 76458-301-08	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/14/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	02/14/2020

Labeler - Circadia by Dr Pugliese, Inc. (013694423)

Establishment
Name	Address	ID/FEI	Business Operations
Circadia by Dr Pugliese, Inc.		013694423	manufacture(76458-301)