Blackmonster Day and Night Moisturizer by BLANK Corporation / EYESOME Co., Ltd.

Blackmonster Day and Night Moisturizer by

Drug Labeling and Warnings

Blackmonster Day and Night Moisturizer by is a Otc medication manufactured, distributed, or labeled by BLANK Corporation, EYESOME Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BLACKMONSTER DAY AND NIGHT MOISTURIZER- sunscreen cream 
BLANK Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Ethylhexyl Methoxycinnamate (7%)

Ethylhexyl Salicylate (5%)

Octocrylene (3%)

Phenylbenzimidazole Sulfonic Acid (3%)

Titanium Dioxide (2.46%)

Sunscreen

■ 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.

■ 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.

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

■ Apply liberally 15 minutes before sun exposure.

■ reapply at least every 2 hours.

■ use a waterresistant 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 of age: Ask a doctor

Water, Propanediol, Ethylhexyl isononanoate, Potassium cetyl phosphate, Niacinamide, Pentylene glycol, Tromethamine, Cetearyl alcohol, Cyclopentasiloxane, Methylene bis-benzotriazolyl tetramethylbutylphenol, Glycerin, Bis-ethylhexyloxyphenol methoxyphenyl triazine, Sorbitan isostearate, Glyceryl stearate, Dimethicone, PEG-100 stearate, Cyclopentasiloxane, Acrylates/C10-30 alkyl acrylate crosspolymer, Carbomer, Pullulan, Aloe barbadensis leaf juice, Aluminum hydroxide, Stearic acid, Decyl glucoside, Caprylyl glycol, Dimethicone/vinyl dimethicone crosspolymer, Allantoin, Butylene glycol, Hydrogenated lecithin, Ethylhexylglycerin, Adenosine, Xanthan gum, Disodium EDTA, Triethoxycaprylylsilane, Hydrolyzed hyaluronic acid, Propylene glycol, Sophora japonica fruit extract, Ethyl hexanediol, Betaine, Panthenol, Glycosyl trehalose, 1,2-Hexanediol, Citric acid, Potassium sorbate, Hydrogenated starch hydrolysate, Sodium benzoate

1 Pumping

Blackmonster day and night

BLACKMONSTER DAY AND NIGHT MOISTURIZER 
sunscreen cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 80718-101
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7 mg  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 mg  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE3 mg  in 100 mL
ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42) ENSULIZOLE3 mg  in 100 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE2.46 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
NIACINAMIDE (UNII: 25X51I8RD4)  
PULLULAN (UNII: 8ZQ0AYU1TT)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
HYDROGENATED STARCH HYDROLYSATE (UNII: 27F77DSJ5V)  
TREHALOSE (UNII: B8WCK70T7I)  
PROPANEDIOL (UNII: 5965N8W85T)  
ETHYLHEXYL ISONONANOATE (UNII: I6KB4GE3K4)  
BISOCTRIZOLE (UNII: 8NT850T0YS)  
GLYCERIN (UNII: PDC6A3C0OX)  
BEMOTRIZINOL (UNII: PWZ1720CBH)  
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PEG-100 STEARATE (UNII: YD01N1999R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
ADENOSINE (UNII: K72T3FS567)  
XANTHAN GUM (UNII: TTV12P4NEE)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ETHOHEXADIOL (UNII: M9JGK7U88V)  
PANTHENOL (UNII: WV9CM0O67Z)  
BETAINE (UNII: 3SCV180C9W)  
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
STYPHNOLOBIUM JAPONICUM FRUIT (UNII: ZI9T58H3S8)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
CARBOMER 940 (UNII: 4Q93RCW27E)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
ALLANTOIN (UNII: 344S277G0Z)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
HYALURONIC ACID (UNII: S270N0TRQY)  
WATER (UNII: 059QF0KO0R)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
TROMETHAMINE (UNII: 023C2WHX2V)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 80718-101-021 in 1 BOX11/03/2020
1NDC: 80718-101-0150 mL in 1 BOTTLE, PLASTIC; Type 7: Separate Products Requiring Cross Labeling
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35211/03/202006/10/2021
Labeler - BLANK Corporation (694619027)

Revised: 6/2021
 

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