Moisturizing Facial Sunscreen

Manufacturer
Neoteric Cosmetics, Inc. | Cosmetic Solutions, LLC
Effective date
2024-10-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:45:19

Label at a glance#

ProductMoisturizing Facial Sunscreen
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Label structure13 sections

Indications and uses

• 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.

Dosage and administration

• After cleansing, apply product to face and neck • Apply liberally 15 minutes before sun exposure • Use a water resistant sunscreen if swimming or sweating • Reapply at least every 2 hours • Children under 6 months of age: Ask a doctor. 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 SP...

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Moisturizing Facial Sunscreen

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.0%

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Homosalate 10.0%,

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octisalate 5.0%

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octocrylene 7.0%

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Oxybenzone 4.5%

(to the right)  

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

• 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

WARNINGS SECTION

• For external use only

• Do not use on damaged or broken skin

OTC - DO NOT USE SECTION

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

• Stop use and ask a doctor if rash occurs

OTC - STOP USE SECTION

• Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

• After cleansing, apply product to face and neck

• Apply liberally 15 minutes before sun exposure

• Use a water resistant sunscreen if swimming or sweating

• Reapply at least every 2 hours

• Children under 6 months of age: Ask a doctor.

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 am-2 pm

• Wear long sleeved shirts, pants, hats and sunglasses.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, C12-15 Alkyl Benzoate, Glyceryl Stearate, PEG-100 Stearate, Glyceryl Dilaurate , Glycerin, Stearic Acid, Propylene Glycol, Sodium Hyaluronate, Hydrolyzed Glycosaminoglycans, Panthenol, Tocopheryl Acetate, Sorbitan Stearate, PEG-40 Stearate, Cetyl Alcohol, Dimethicone, Vinyl Dimethicone Crosspolymer, Silica, BHT, Triethanolamine, Diazolidinyl Urea, Iodopropynyl Butylcarbamate, Disodium EDTA, Carbomer

Other Information

OTHER SAFETY INFORMATION

• Protect this product from excessive heat and direct sun.

MANUFACTURED BY NEOTERIC COSMETICS, INC., DENVER, CO 80239

BOTTOM

UPC

BOTTOM RIGHT PANEL TAB

(Item Number) 840181

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ALPHA
Skin Care
Moisturizing
Facial Sunscreen
SPF 30

PRINCIPAL DISPLAY PANEL ALPHA Skin Care Moisturizing Facial Sunscreen SPF 30PRINCIPAL DISPLAY PANEL ALPHA Skin Care Moisturizing Facial Sunscreen SPF 30

FDA-Initiated Inactive NDC Indexing#

Products#

Every source-derived product name is available through these pages.

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62673-16462673-164-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
23e91dc8-9a0f-5e59-e063-6294a90a1e527e9821f1-2c1b-41e9-b161-4d2803fbb8392024-10-07WarningsExact identifier
spl id: 23e91dc8-9a0f-5e59-e063-6294a90a1e52
spl set id: 7e9821f1-2c1b-41e9-b161-4d2803fbb839

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.