MYDERM HYDRATING SUNSCREEN BROAD SPECTRUM SPF 50- avobenzone, homosalate, octisalate, octocrylene spray

MyDerm Hydrating Sunscreen Broad Spectrum SPF 50 by

Drug Labeling and Warnings

MyDerm Hydrating Sunscreen Broad Spectrum SPF 50 by is a Otc medication manufactured, distributed, or labeled by Inspec Solutions. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Avobenzone 3.0%

Homosalate 15%

Octisalate 5%

Octocrylene 10%

WHEN USING

When using this product:

keep out of eyes. Rinse with water to remove.

Keep away from face to avoid breathing it.

Do not puncture or incinerate, Contents under pressure

Do not store at temperature above 120⁰F

Stop use and ask a doctor if rash occurs.

PURPOSE

Avobenzone 3.0% ……………………………………………………………………………… Sunscreen

Homosalate 15.0% ……………………………………………………………………………. Sunscreen

Octisalate 5.0% …………………………………………………………………………………. Sunscreen

Octocrylene 10.0% ……………………………………………………………………………. Sunscreen

STOP USE

Stop use and ask a doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT

Inactive Ingredients

Acrylates/Octylacrylamide Copolymer

Alcohol Denat

Aloe Vera Oil Extract

Caprylic/Capric Triglyceride

Diethylhexyl Syringylidenemalonate

Glycerin

Tocopheryl Acetate

Retinyl Palmitate

WHEN USING

keep out of eyes. Rinse with water to remove.

Keep away from face to avoid breathing it.

Do not puncture or incinerate, Contents under pressure

Do not store at temperature above 120⁰F

Stop use and ask a doctor if rash occurs.

WARNINGS

Warnings

For External use only.

INDICATIONS & USAGE

For external use only

DOSAGE & ADMINISTRATION

See Direction section for Dosage & Administration

MyDerm Hydrating Sunscreen Spray Broad Spectrum SPF 50

INGREDIENTS AND APPEARANCE

MYDERM HYDRATING SUNSCREEN BROAD SPECTRUM SPF 50 
avobenzone, homosalate, octisalate, octocrylene spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72667-075
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	15 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	10 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK)
ALCOHOL (UNII: 3K9958V90M)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72667-075-01	142 mL in 1 CAN; Type 0: Not a Combination Product	03/08/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	03/01/2024

Labeler - Inspec Solutions (081030372)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions		081030372	manufacture(72667-075)