SOME BY MI V10 HYAL AIR FIT SUNSCREEN- sunscreent cream

SOME BY MI V10 HYAL AIR FIT SUNSCREEN by

Drug Labeling and Warnings

SOME BY MI V10 HYAL AIR FIT SUNSCREEN by is a Otc medication manufactured, distributed, or labeled by PERENNEBELL, reBom Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Directions
■ Apply liberally 15 minutes before sun exposure.

■ Children under 6 months of age: Ask a doctor.

■ 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.

■ See Outer Package for complete Drug Facts.

INDICATIONS & USAGE

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.

INACTIVE INGREDIENT

Water, Butyloctyl Salicylate, Dicaprylyl Carbonate, Cetearyl Alcohol, Dipropylene Glycol, Cetearyl Glucoside, Poly C10-30 Alkyl Acrylate, Sorbitan Olivate, Polymethylsilsesquioxane, Niacinamide, Benzyl Glycol, Glyceryl Stearate SE, Butylene Glycol, Panthenol, Arginine, Carbomer, Brassica Oleracea Italica (Broccoli) Extract, Melaleuca Alternifolia [Tea Tree) Leaf Extract, Hydroxypropyl Methylcellulose Stearoxy Ether, Centella Asiatica Extract, Camellia Sinensis Leaf Water, Tocopherol, Disodium EDTA, Ethylhexylglycerin, Xanthan Gum, Adenosine, 1,2-Hexanediol, Bambusa Vulgaris Leaf Extract, Oldenlandia Diffusa Extract, Lonicera Caprifolium (Honeysuckle] Extract, Yeast Extract, Limonia Acidissima Extract, Sodium Hyaluronate, Propanediol, Sodium Hyaluronate Crosspolymer, Ascorbyl Propyl Hyaluronate, Hydrolyzed Glycosaminoglycans, Glycerin, Madecassic Acid, Asiaticoside, Asiatic Acid, Caprylyl Glycol, Sodium Ascorbyl Phosphate, Hydrolyzed Hyaluronic Acid, Hyaluronic Acid, Biotin, Cyanocobalamin, Ascorbic Acid, Folic Acid, Thiamine HCI, Riboflavín, Pyridoxine, Fragrance, Citral, Benzyl Salicylate, Linalool, Limonene

ACTIVE INGREDIENT

Avobenzone 3%

Homosalate 10%

Octisalate 5%

Octocrylene 8.7%

PURPOSE

Sunscreen

KEEP OUT OF REACH OF CHILDREN

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

WARNINGS

For external use only

INSTRUCTIONS FOR USE

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.

OTHER SAFETY INFORMATION

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

■ Sun alert: Limitng sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun.

DO NOT USE

Do not use on damaged or broken skin.

STOP USE

Stop use and ask a doctor if rash occurs.

WHEN USING

When using this product keep out of eyes. Rinse with water to remove.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOME BY MI V10 HYAL AIR FIT SUNSCREEN 
sunscreent cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74472-235
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 50 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	10 g  in 50 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 50 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	8.7 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	27.585 mL  in 50 mL

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74472-235-01	1 in 1 CASE	07/31/2023
1		50 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	07/31/2023

Labeler - PERENNEBELL (694788814)

Registrant - PERENNEBELL (694788814)

Establishment
Name	Address	ID/FEI	Business Operations
reBom Co., Ltd.		695951708	manufacture(74472-235)