DERMA SOLEIL NATURAL AGE-FREE FACIAL SUNBLOCK SPF 30- octocrylene,octyl methoxycinnamate,octyl salicylate,oxybenzone lotion

DERMA SOLEIL NATURAL AGE-FREE FACIAL SUNBLOCK SPF 30 by

Drug Labeling and Warnings

DERMA SOLEIL NATURAL AGE-FREE FACIAL SUNBLOCK SPF 30 by is a Otc medication manufactured, distributed, or labeled by Deserving Health International Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Octocrylene 4%
Octyl Methoxycinnamate 7.5%,
Octyl Salicylate 4%,
Oxybenzone 5%

PURPOSE

Sunscreen

DOSAGE & ADMINISTRATION

WHEN USING

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

For external use only.

Do not use on damaged or broken skin. Stop use and ask a doctor if rash occurs.

When using this product keep out of eyes. Rinse with water to remove.

Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

ASK DOCTOR

KEEP OUT OF REACH OF CHILDREN

INACTIVE INGREDIENT

Aloe Vera Gel, C12-15 Alkyl Benzoate, Aqua and Glycerin and Sodium Levulinate and Sodium Anisate, Fragrance, Acrylates/C10-30 Alkyl Acrylates Crosspolymer, Aminomethyl Propanol, Carbomer, Titanium Dioxide, Hydroxypropyl Methylcellulose, Tetrasodium EDTA, Evening Primrose Oil, Avocado Oil, Jojoba Oil, Grape Seed Oil, Blue Chamomile Oil, Calendula Oil, Hydrolyzed Wheat Protein, Retinyl Palmitate, Ascorbic Acid, Tocopherol Acetate.

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DERMA SOLEIL NATURAL AGE-FREE FACIAL SUNBLOCK SPF 30 
octocrylene,octyl methoxycinnamate,octyl salicylate,oxybenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69711-905
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	5 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	4 g  in 100 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7.5 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
EDETATE SODIUM (UNII: MP1J8420LU)
JOJOBA OIL (UNII: 724GKU717M)
GRAPE SEED OIL (UNII: 930MLC8XGG)
EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
SODIUM ANISATE (UNII: F9WFJ28MV9)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
HYDROLYZED WHEAT PROTEIN (ENZYMATIC; 3000 MW) (UNII: J2S07SB0YL)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
SODIUM LEVULINATE (UNII: VK44E1MQU8)
AVOCADO OIL (UNII: 6VNO72PFC1)
CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
HYPROMELLOSES (UNII: 3NXW29V3WO)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69711-905-01	120 mL in 1 TUBE; Type 0: Not a Combination Product	02/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	02/21/2020

Labeler - Deserving Health International Corp. (079767886)

Establishment
Name	Address	ID/FEI	Business Operations
Deserving Health International Corp.		202617023	manufacture(69711-905)