Manefit Bling Bling Whitening Platinum Hydrogel Mask by Imine Co., Ltd. 59401-004_Deactivation

Manefit Bling Bling Whitening Platinum Hydrogel Mask by

Drug Labeling and Warnings

Manefit Bling Bling Whitening Platinum Hydrogel Mask by is a Otc medication manufactured, distributed, or labeled by Imine Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MANEFIT BLING BLING WHITENING PLATINUM HYDROGEL MASK- niacinamide cream 
Imine Co., Ltd.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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59401-004_Deactivation

Niacinamide (2 %)

Immediately nourishes your skin, resulting in a noticeably brighter, softer, and smoother complexion.

For external use only.

Apply one mask sheet at a time.

Skin Protectant

After cleansing and applying toner, remove sheet mask from packaging and place carefully around eyes and nose. Relax for 20 minutes. Remove mask and discard.

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

Stop use and ask a doctor if rash occurs.

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

Do not use on damaged or broken skin.

Water, Butylene Glycol, Glycerin, Citrus Paradisi (Grapefruit) Fruit Extract, Ceratonia Siliqua Gum, Chondrus Crispus (Carrageenan), Sodium Polyacrylate, Cellulose Gum, Hydrogenated Polydecene, Disodium EDTA, Phenoxyethanol, Mica, Polysorbate 20, Titanium Dioxide, Alumina, Trideceth-6, Glass, Triethoxycaprylylsilane, Sea Water, Jania Rubens Extract, Platinum Powder(10ppm), Tin Oxide

MANEFIT BLING BLING WHITENING PLATINUM HYDROGEL MASK 
niacinamide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59401-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	0.6 g  in 30 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCERIN (UNII: PDC6A3C0OX)
GRAPEFRUIT (UNII: O82C39RR8C)
LOCUST BEAN GUM (UNII: V4716MY704)
CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE DISODIUM (UNII: 7FLD91C86K)
MICA (UNII: V8A1AW0880)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
ALUMINUM OXIDE (UNII: LMI26O6933)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
PLATINUM (UNII: 49DFR088MY)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
TRIDECETH-6 (UNII: 3T5PCR2H0C)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59401-004-01	30 g in 1 POUCH; Type 0: Not a Combination Product	09/07/2015	12/26/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/07/2015	12/26/2019

Labeler - Imine Co., Ltd. (557816813)

Registrant - Imine Co., Ltd. (557816813)

Establishment
Name	Address	ID/FEI	Business Operations
i Mine Co.,Ltd.		557816813	manufacture(59401-004)

Revised: 12/2019

Document Id: 9aa42679-4473-6b71-e053-2a95a90a5a83

34390-5

Set id: add7f542-70f3-4b05-be4e-25c2ec20231a

Version: 3

Effective Time: 20191226

 

Imine Co., Ltd.