DAILY SUPERGOOP DOSE BIORETINOL MINERAL SPF 40- daily dose bioretinol mineral spf 40 lotion

DAILY SUPERGOOP DOSE BIORETINOL MINERAL SPF 40 by

Drug Labeling and Warnings

DAILY SUPERGOOP DOSE BIORETINOL MINERAL SPF 40 by is a Otc medication manufactured, distributed, or labeled by MANA Products, INC, MANA Products,Inc, MANA Products, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Zinc Oxide 16.5%

Purpose

Sunscreen

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

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. Stop use and ask a doctor if rash occurs.

Keep out of the Reach of Children

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

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 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

Other Information

Protect the product in this container from excessive heat and direct sun

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DAILY SUPERGOOP DOSE BIORETINOL MINERAL SPF 40 
daily dose bioretinol mineral spf 40 lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59735-614
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
TOCOPHEROL (UNII: R0ZB2556P8)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
PEG-6 SORBITAN OLEATE (UNII: 58O7V09UCI)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
VITIS VINIFERA SEED (UNII: C34U15ICXA)
PROPANEDIOL (UNII: 5965N8W85T)
BAKUCHIOL (UNII: OT12HJU3AR)
QUERCUS ROBUR TWIG BARK (UNII: 2JFK226947)
CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)
OLIVE OIL POLYGLYCERYL-6 ESTERS (UNII: 4KDO9AFM9I)
VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
POLYGLYCERYL-6 DIOLEATE (UNII: 062SZD3F3X)
ISODODECANE (UNII: A8289P68Y2)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
QUERCUS ROBUR WOOD (UNII: 1B1CMC06QJ)
ISOHEXADECANE (UNII: 918X1OUF1E)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)
WATER (UNII: 059QF0KO0R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
GLYCERIN (UNII: PDC6A3C0OX)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
CARNOSINE (UNII: 8HO6PVN24W)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59735-614-01	1 in 1 BOX	10/18/2022
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 59735-614-02	6.5 mL in 1 BOTTLE; 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 - MANA Products, INC (078870292)

Establishment
Name	Address	ID/FEI	Business Operations
MANA Products,Inc		032870270	manufacture(59735-614)

Establishment
Name	Address	ID/FEI	Business Operations
MANA Products, Inc		078870292	manufacture(59735-614)