DECREE DAILY SHIELD BROAD SPECTRUM SPF 30 SUNSCREEN- titanium dioxide and zinc oxide liquid

Decree Daily Shield Broad Spectrum SPF 30 Sunscreen by

Drug Labeling and Warnings

Decree Daily Shield Broad Spectrum SPF 30 Sunscreen by is a Otc medication manufactured, distributed, or labeled by Cosmetic Solutions LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

DRUG FACTS:

ACTIVE INGREDIENTS

Titanium Dioxide - 7.2%, Zinc Oxide - 4.0%

PURPOSE

Sunscreen

USES

Helps prevent sunburn.

WARNINGS

For external use only.

When using this product keep away from face to avoid breathing it.

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.

Danger

Flammable. Contents under pressure. Do not use near fire, heat or while smoking. Do not puncture or incinerate. Store at temperature below 120°F (48°C). Use only as directed. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

DIRECTIONS

For sunscreen use:

spray liberally and spread evenly by hand 15 minutes before sun exposure.

• - hold container 4 to 6 inches from the skin to apply.
• - do not spray directly into face. Spray on hands then apply to face.
• - do not apply in windy conditions.
• - use in a well-ventilated area.

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.
• - reapply at least every 2 hours.
• - use a water resistant sunscreen if swimming or sweating.

INACTIVE INGREDIENTS

Water, Butyloctyl Salicylate, Glycerin, Dimethicone, Caprylic/Capric Triglyceride, Propanediol, Polyglyceryl-10 Oleate, Coco-Caprylate/Caprate, Rosa Damascena Flower Water, Polyhydroxystearic Acid, Phenoxyethanol, Aluminum Stearate, Carthamus Tinctorius Oleosomes, Alumina, Butylene Glycol, Polyglyceryl-2 Caprate, Microcrystalline Cellulose, Potassium Cetyl Phosphate, Polyglyceryl-3 Polyricinoleate, Hydrolyzed Wheat Protein/PVP Crosspolymer, Simmondsia Chinensis Seed Oil, Stearic Acid, Sucrose Stearate, Marrubium Vulgare Meristem Cell Culture, Polyglyceryl-3 Diisostearate, Ethylhexylglycerin, Cellulose Gum, Glyceryl Caprylate, Squalane, Triethoxycaprylylsilane, Camellia Sinensis Leaf Extract, Carbomer, Polysorbate 20, Aspalathus Linearis Extract, Palmitoyl Tripeptide-1, Xanthan Gum, Palmitoyl Tetrapeptide-7.

OTHER INFORMATION

Protect the product in this container from excessive heat and direct sun.

PRINCIPAL DISPLAY PANEL - 75 ML Can Label

Day Shield
DAILY / AM + PM
UV SHIELD
SPRAY SOLAIRE
BROAD SPECTRUM SPF 30
SUNSCREEN

D
E
C
R
E
E

BY DR AJ STURNHAM

75ML e 2.53 FL OZ

INGREDIENTS AND APPEARANCE

DECREE DAILY SHIELD BROAD SPECTRUM SPF 30 SUNSCREEN 
titanium dioxide and zinc oxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66163-3919
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Titanium Dioxide (UNII: 15FIX9V2JP) (Titanium Dioxide - UNII:15FIX9V2JP)	Titanium Dioxide	7.2 g  in 100 mL
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z)	Zinc Oxide	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHICONE (UNII: 92RU3N3Y1O)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
PROPANEDIOL (UNII: 5965N8W85T)
POLYGLYCERYL-10 OLEATE (UNII: 55C81W76DH)
COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)
ROSA X DAMASCENA FLOWER OIL (UNII: 18920M3T13)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALUMINUM STEARATE (UNII: U6XF9NP8HM)
CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309)
ALUMINUM OXIDE (UNII: LMI26O6933)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
POLYGLYCERYL-2 CAPRATE (UNII: JX7WXJ41DH)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
JOJOBA OIL (UNII: 724GKU717M)
STEARIC ACID (UNII: 4ELV7Z65AP)
SUCROSE STEARATE (UNII: 274KW0O50M)
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
SQUALANE (UNII: GW89575KF9)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
XANTHAN GUM (UNII: TTV12P4NEE)
PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66163-3919-1	75 mL in 1 CAN; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	05/01/2020

Labeler - Cosmetic Solutions LLC (807907928)