CUROLOGY DAILY MOISTURIZING SUNSCREEN SPF 30- avobenzone, homosalate, octisalate, octocrylene cream

Curology Daily Moisturizing Sunscreen SPF 30 by

Drug Labeling and Warnings

Curology Daily Moisturizing Sunscreen SPF 30 by is a Otc medication manufactured, distributed, or labeled by Curology, Dermaceutical Laboratories Limited Liability Company, Dermaceutical Laboratories, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Avobenzone 1.5%
Homosalate 5%
Octisalate 4%
Octocrylene 6%

Purpose

Sunscreen

Uses

Helps prevent sunburn

Warnings

For external use only.

Keep out of reach of children.

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

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.

Directions

• apply generously 15 minutes before sun exposure
• reapply 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
• children under 6 months of of age: Ask a doctor

Other information

• store at 20°-25° (68°-77°F)
• protect the product in this container from excessive heat and direct sun

Inactive ingredients

Water, Methyl Trimethicone, Propanediol, Silica, Glycerin, Butyloctyl Salicylate, Ammonium Acryloyldimethyltaurate/VP Copolymer, 1,2-Hexanediol, Glyceryl Oleate Citrate, Polyacrylate-13, Polyisobutene, Caprylhydroxamic Acid, Trisodium Ethylenediamine Disuccinate, Niacinamide, Panthenol, Zinc PCA, Sodium Citrate, Tocopheryl Acetate, Polysorbate 20

Package Labeling:

INGREDIENTS AND APPEARANCE

CUROLOGY DAILY MOISTURIZING SUNSCREEN SPF 30 
avobenzone, homosalate, octisalate, octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82575-036
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	15 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	50 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	OCTISALATE	40 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	60 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
METHYL TRIMETHICONE (UNII: S73ZQI0GXM)
PROPANEDIOL (UNII: 5965N8W85T)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
GLYCERYL MONOOLEATE CITRATE (UNII: NLE5KIG74K)
POLYACRYLATE-13 (UNII: FS2D4T67EA)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
NIACINAMIDE (UNII: 25X51I8RD4)
PANTHENOL (UNII: WV9CM0O67Z)
ZINC PIDOLATE (UNII: C32PQ86DH4)
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
POLYSORBATE 20 (UNII: 7T1F30V5YH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82575-036-00	1 in 1 CARTON	07/01/2025
1		50 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 Drug	M020	07/01/2025

Labeler - Curology (104103284)

Registrant - Dermaceutical Laboratories Limited Liability Company (078457159)

Establishment
Name	Address	ID/FEI	Business Operations
Dermaceutical Laboratories Limited Liability Company		078457159	manufacture(82575-036)

Establishment
Name	Address	ID/FEI	Business Operations
Dermaceutical Laboratories, LLC		080375664	manufacture(82575-036)