by Selected Daily Broad Spectrum Sunscreen

Manufacturer
Garam Of Nature
Effective date
2021-08-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:41:45

Label at a glance#

Productby Selected Daily Broad Spectrum Sunscreen
Active ingredientOCTINOXATE, OCTISALATE
Label structure10 sections

Indications and uses

■ helps prevent sunburn ■ it 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

■ Apply liberally and spread evenly by hand 15 minutes before sun exposure•reapply:•after 80 minutes of swimming or sweating•immediately after towel drying • at least every 2 hours•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 of 15 or higher and other sun protection measures incl...

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Ethylhexyl Methoxycinnamate 7.0%
Ethylhexyl Salicylate 4.0%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Dipropylene Glycol, Butylene Glycol, Ethylhexyl Palmitate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Cetearyl Alcohol, Dibutyl Adipate, Ethylhexyl Triazone, Glyceryl Stearate, Hexyl Laurate,  olyglyceryl-3 Methylglucose Distearate, Polysorbate 60, C14-22 Alcohols, PEG-100 Stearate, 1,2-Hexanediol, Limonia Acidissima Extract, Hydroxyacetophenone, Silica, Fragrance, C12-20 Alkyl Glucoside, Carbomer, Dimethicone, Tromethamine, Ophiopogon Japonicus Root  Extract, Panax Ginseng Root Extract, Schisandra Chinensis Fruit Extract, Ammonium Acryloyldimethyltaurate/VP Copolymer, Disodium EDTA, 
Ipomoea Purpurea Extract, Lilium Candidum Flower Extract, Magnolia Liliflora Flower Extract, Paeonia Albiflora Flower Extract

PURPOSE

OTC - PURPOSE SECTION

Sunscreen

WARNINGS

WARNINGS SECTION

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 ask a doctor if rash occurs

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

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical help or contact a Posion Control Center right away

Uses

INDICATIONS & USAGE SECTION

■ helps prevent sunburn
■ it used as directed with other sun protection measures (see Directions). Decreases the risk of skin cancer and early skin aging caused by the sun

Directions

DOSAGE & ADMINISTRATION SECTION

■ Apply liberally and spread evenly by hand 15 minutes before sun exposure•reapply:•after 80 minutes of swimming or sweating•immediately after towel drying • at least every 2 hours•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 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-sleeve shirts, pants, hats, and sunglasses
• children under 6 months: Ask a docto

Other Information

OTHER SAFETY INFORMATION

■ Do not store this product in an inappropriate place such as high or low temperatures or under direct sun light

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73509-050-01by Selected Daily Broad Spectrum Sunscreen50 mL in 1 TUBECREAM501
73509-050-02by Selected Daily Broad Spectrum Sunscreen1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73509-050BY SELECTED DAILY BROAD SPECTRUM SUNSCREEN (ETHYLHEXYL METHOXYCINNAMATE, ETHYLHEXYL SALICYLATE) CREAM [GARAM OF NATURE]1Legacy NDC, 2 package rows20210803_d218a8de-e996-4e5e-a931-b29017909b78.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73509-05073509-050-01, 73509-050-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
4583c1dc-5c2d-4794-bce0-75962fdd4a9bd218a8de-e996-4e5e-a931-b29017909b782021-08-03WarningsExact identifier
spl id: 4583c1dc-5c2d-4794-bce0-75962fdd4a9b
spl set id: d218a8de-e996-4e5e-a931-b29017909b78

Reported adverse events (FAERS/openFDA)#

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