Daily Dose Bioretinol Mineral SPF 40

Manufacturer
Supergoop, LLC
Effective date
2026-01-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
monthly-update
Hydrated at
2026-06-03 17:51:48

Label at a glance#

ProductDaily Dose Bioretinol Mineral SPF 40
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 16.5% Sunscreen

OTC - PURPOSE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INDICATIONS & USAGE SECTION

Stop use and ask a doctor if rash occurs.

WARNINGS SECTION

For External use only

Do not use on damaged or broken skin

When using this product, Keep our of eyes. Rinse with water to remove

DOSAGE & ADMINISTRATION SECTION

Directions

• apply generously and evenly 15 minutes before sun exposure
• reapply at least every 2 hours
• use a water resistant sunscreen if swimming or sweating

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 a.m. - 2 p.m. ◦ Wear long-sleeved shirts, pants, hats, and sunglasses • Children under 6 months: Ask a doctor

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Aqua/Water/Eau, Dicaprylyl Ether, Caprylic/Capric Triglyceride, Butyloctyl Salicylate, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Silica, Olive Oil Polyglyceryl-6 Esters, Isohexadecane, Glycerin, Sorbitan Oleate, VP/Hexadecene Copolymer, Polyhydroxystearic acid, Polyglyceryl-6 Pentaoleate, Propanediol, Bakuchiol, Ethylhexylglycerin, Isododecane, Sodium Chloride, Tocopherol, Disteardimonium Hectorite, Camellia Sinensis Leaf Extract, Propylene Carbonate, Quercus Robur Bark Extract, Quercus Robur Wood Extract, Vitis Vinifera (Grape) Seed Extract, Carnosine, Trisodium Ethylenediamine Disuccinate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Daily Dose Bioretinol + Mineral SPF

SPF 40

Broad Spectrum Sunscreen Fluid

1 fl. oz. / 30 mL

CartonCarton

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75936-604-01Daily Dose Bioretinol Mineral SPF 4030 mL in 1 BOTTLELIQUID303
75936-604-02Daily Dose Bioretinol Mineral SPF 401 in 1 BOXLIQUID13
75936-604-03Daily Dose Bioretinol Mineral SPF 406.5 mL in 1 BOTTLELIQUID6.53
75936-604-04Daily Dose Bioretinol Mineral SPF 401.5 mL in 1 PACKETLIQUID1.53

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75936-60475936-604-01, 75936-604-02, 75936-604-03, 75936-604-04

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22024-12-05full-release2026-06-01 00:41:11

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
Daily Dose Bioretinol Mineral SPF 40ZINC OXIDESupergoop, LLCeb5bbc70-dbdf-06a8-e053-2995a90a66c12026-01-09WarningsExact identifier
ndc (package): 75936-604-01
ndc (package): 75936-604-03
ndc (package): 75936-604-02
ndc (package): 75936-604-04
ndc (product): 75936-604
ndc11 (package): 75936060403
ndc11 (package): 75936060401
ndc11 (package): 75936060404
ndc11 (package): 75936060402
spl id: 47fc1ad0-97d7-755a-e063-6394a90a118a
spl set id: eb5bbc70-dbdf-06a8-e053-2995a90a66c1

Reported adverse events (FAERS/openFDA)#

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