MOOR SPA SPF30 Sunscreen by Derma Soleil / Deserving Health International Corp.

MOOR SPA SPF30 Sunscreen by

Drug Labeling and Warnings

MOOR SPA SPF30 Sunscreen by is a Otc medication manufactured, distributed, or labeled by Derma Soleil, Deserving Health International Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MOOR SPA SPF30 SUNSCREEN- titanium dioxide,zinc oxide cream 
Derma Soleil

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MOOR SPA SPF 30+ Lotion

80 mL NDC: 69711-351-01

Sunscreen

Micronized Zinc Oxide 11%

Micronized Titanium Dioxide 8%

The sun may cause sunburn, premature aging of the skin and skin cancer. Avoiding the sun, wearing protective clothing and regular use of sunscreens over the years reduces the chance of these harmful effects.

Helps prevent sunburn

If used as directed with other sun protection measures, decreases the risk of skin cancer and early skin aging caused by sun

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 consult a doctor if rash occurs.

Keep out of reach of children.

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

Apply liberally 15 minutes before sun exposure

Reapply

After 40 minutes of swimming or sweating

immediately after towel drying

at least every 2 hours

Children under 6 months of age: ask a doctor

Water, Coco-Caprylate, Dicaprylyl Carbonate, Lauryl Glucoside,

Polyglyceryl-2 Dipolyhydroxystearate, Glycerin, Microcrystalline Cellulose,

Cellulose Gum, Green Tea Extract, DL-Panthenol, Sodium Ascorbyl Phosphate,

D-alpha Tocopheryl Acetate, Phytic Acid, Triethoxycaprylylsilane, Polyhydroxystearic Acid,

Xanthan Gum, Benzyl Alcohol, Ethylhexylglycerin, D-alpha Tocopherol

MOOR SPA SPF30 SUNSCREEN 
titanium dioxide,zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69711-351
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	11 g  in 100 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	8 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
GLYCERIN (UNII: PDC6A3C0OX)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
WATER (UNII: 059QF0KO0R)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
PANTHENOL (UNII: WV9CM0O67Z)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
TOCOPHERYL NICOTINATE, D-.ALPHA. (UNII: WI1J5UCY5C)
FYTIC ACID (UNII: 7IGF0S7R8I)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
BENZYL ALCOHOL (UNII: LKG8494WBH)
CARBOXYMETHYLCELLULOSE CALCIUM (UNII: UTY7PDF93L)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69711-351-01	80 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/12/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	09/12/2023	12/19/2023

Labeler - Derma Soleil (079767886)

Establishment
Name	Address	ID/FEI	Business Operations
Deserving Health International Corp.		202617023	manufacture(69711-351)

Revised: 12/2023

Document Id: 0cdb8b07-f13e-c66b-e063-6294a90a7acb

34390-5

Set id: 05396b74-03c4-2700-e063-6394a90acf9d

Version: 2

Effective Time: 20231219

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