DAILY DOSE BIORETINOL MINERAL SPF 40- zinc oxide liquid

Daily Dose Bioretinol Mineral SPF 40 by

Drug Labeling and Warnings

Daily Dose Bioretinol Mineral SPF 40 by is a Otc medication manufactured, distributed, or labeled by Supergoop, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Zinc Oxide 16.5% Sunscreen

PURPOSE

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

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

Stop use and ask a doctor if rash occurs.

WARNINGS

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

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

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

PRINCIPAL DISPLAY PANEL

Daily Dose Bioretinol + Mineral SPF

SPF 40

Broad Spectrum Sunscreen Fluid

1 fl. oz. / 30 mL

INGREDIENTS AND APPEARANCE

DAILY DOSE BIORETINOL MINERAL SPF 40 
zinc oxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75936-604
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	16.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
QUERCUS ROBUR TWIG BARK (UNII: 2JFK226947)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
TOCOPHEROL (UNII: R0ZB2556P8)
CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
QUERCUS ROBUR WOOD (UNII: 1B1CMC06QJ)
WATER (UNII: 059QF0KO0R)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
OLIVE OIL POLYGLYCERYL-6 ESTERS (UNII: 4KDO9AFM9I)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
ISOHEXADECANE (UNII: 918X1OUF1E)
GLYCERIN (UNII: PDC6A3C0OX)
POLYGLYCERYL-6 DIOLEATE (UNII: 062SZD3F3X)
PEG-6 SORBITAN OLEATE (UNII: 58O7V09UCI)
VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
VITIS VINIFERA SEED (UNII: C34U15ICXA)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
PROPANEDIOL (UNII: 5965N8W85T)
BAKUCHIOL (UNII: OT12HJU3AR)
ISODODECANE (UNII: A8289P68Y2)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
CARNOSINE (UNII: 8HO6PVN24W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75936-604-02	1 in 1 BOX	10/18/2022
1	NDC: 75936-604-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 75936-604-03	6.5 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/18/2022
3	NDC: 75936-604-04	1.5 mL in 1 PACKET; Type 0: Not a Combination Product	10/18/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	10/18/2022

Labeler - Supergoop, LLC (117061743)