MINORI DAILY MINERAL FACE SUNSCREEN BROAD SPECTRUM SPF 30- zinc oxide lotion

Minori Daily Mineral Face Sunscreen by

Drug Labeling and Warnings

Minori Daily Mineral Face Sunscreen by is a Otc medication manufactured, distributed, or labeled by Minori Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ZINC OXIDE 10%

PURPOSE

SUNSCREEN

USE

• HELPS PREVENT SUNBURN

WARNINGS

• 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 SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

• APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE.
• CHILDREN UNDER 6 MONTHS OF AGE: ASK A DOCTOR.
• USE A WATER-RESISTANT SUNSCREEN IF SWIMMING OR SWEATING.
• REAPPLY 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 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.

OTHER INFORMATION

• PROTECT THE PRODUCT IN THIS CONTAINER FROM EXCESSIVE HEAT AND DIRECT SUN.

INACTIVE INGREDIENTS

Water, Butylene Glycol, Caprylic/Capric Triglyceride, Dimethicone, Cetearyl Alcohol, Cetearyl Olivate, Polyglyceryl-3 Diisostearate, Sorbitan Olivate, Chamomilla Recutita (Matricaria) Flower Extract, Aloe Barbadensis (Aloe Vera) Leaf Juice, Punica Granatum Fruit Extract, Cetearyl Glucoside, Triethoxycaprylylsilane, Tocopheryl Acetate, Xanthan Gum, Glycerin, Phenoxyethanol, Ethylhexylglycerin, Iron Oxides.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MINORI DAILY MINERAL FACE SUNSCREEN  BROAD SPECTRUM SPF 30
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84321-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	10 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CETEARYL OLIVATE (UNII: 58B69Q84JO)
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
POMEGRANATE (UNII: 56687D1Z4D)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
FERRIC OXIDE RED (UNII: 1K09F3G675)
WATER (UNII: 059QF0KO0R)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
DIMETHICONE (UNII: 92RU3N3Y1O)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
SORBITAN OLIVATE (UNII: MDL271E3GR)
CHAMOMILE (UNII: FGL3685T2X)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
XANTHAN GUM (UNII: TTV12P4NEE)
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84321-101-12	1 in 1 BOX	07/15/2024
1	NDC: 84321-101-11	50 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 84321-101-14	1 in 1 BOX	07/15/2024
2	NDC: 84321-101-13	10 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	07/15/2024

Labeler - Minori Inc. (117564136)