Sallys Box Delight Collagen Hydrogel Mask by Imine Co., Ltd 59401-015_Deactivation

Sallys Box Delight Collagen Hydrogel Mask by

Drug Labeling and Warnings

Sallys Box Delight Collagen Hydrogel Mask by is a Otc medication manufactured, distributed, or labeled by Imine Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SALLYS BOX DELIGHT COLLAGEN HYDROGEL MASK- allantoin 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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59401-015_Deactivation

Allantoin (0.005%)

Moisturizing + Lifting

Use with caution if you are highly sensitive to any bandages or wet compresses.

Apply one mask sheet at a time.

Skin Protectant

1. After cleansing your face, apply some skin toner. 2. Open the package and remove the protective upper and lower films. 3. Apply the mask sheets evenly on your face keeping the eye and mouth area clear. 4. Remove the mask in about 30 minutes and gently use your fingers to pat any remaining product into the skin until thoroughly absorbed. *Apply the lower sheet first. *Place the side where the protective film was on your skin.

Keep out of reach of children.

If any signs of the following skin troubles appear, discontinue use and talk to your dermatologist as it may aggravate the condition. 1) If any conditions such as rash, swelling, itching, or irritation occur when using the product. 2) If sunlight exposure to an area of skin to which the product is applied causes skin irritation as above.

Avoid contact with eyes. In case of contact with eyes, rinse immediately with water.

Do not use the product on an open skin wound or on areas of eczema or infection.

Water, Glycerin, Butylene Glycol, Caprylic/Capric Triglyceride, Citrus Paradisi (Grapefruit) Fruit Extract, Ceratonia Siliqua Gum, Chondrus Crispus (Carrageenan), Cellulose Gum, Sodium Polyacrylate, Hydrolyzed Collagen, Hydrogenated Polydecene, Polysorbate 20, Mannan, Trideceth-6, Portulaca Grandiflora Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Mentha Piperita (Peppermint) Leaf Extract, Lavandula Angustifolia (Lavender) Extract , Chamomilla Recutita (Matricaria) Flower Extract, Camellia Sinensis Leaf Extract , Paeonia Albiflora Root Extract , Jasminum Officinale (Jasmine) Extract , Mentha Viridis (Spearmint) Extract , Scutellaria Baicalensis Root Extract, Sodium Hyaluronate, Disodium EDTA, Phenoxyethanol, Fragrance, CI 42090

SALLYS BOX DELIGHT COLLAGEN HYDROGEL MASK 
allantoin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59401-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.0125 mg  in 25 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCERIN (UNII: PDC6A3C0OX)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
GRAPEFRUIT (UNII: O82C39RR8C)
LOCUST BEAN GUM (UNII: V4716MY704)
CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
PORK COLLAGEN (UNII: I8442U2G7J)
HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
YEAST MANNAN (UNII: 91R887N59P)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
PORTULACA GRANDIFLORA SEED (UNII: 73NV03RHQT)
ROSEMARY (UNII: IJ67X351P9)
MENTHA PIPERITA LEAF (UNII: A389O33LX6)
LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
CHAMOMILE (UNII: FGL3685T2X)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
JASMINUM OFFICINALE FLOWER (UNII: 0Q8K841432)
MENTHA SPICATA (UNII: O2H83I4PUN)
SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
CAMELLIA JAPONICA SEED OIL (UNII: U37N0S910T)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59401-015-01	25 g in 1 POUCH; Type 0: Not a Combination Product	12/02/2014	12/27/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/02/2014	12/27/2019

Labeler - Imine Co., Ltd (557816813)

Registrant - Imine Co., Ltd (557816813)

Establishment
Name	Address	ID/FEI	Business Operations
i Mine Co.,Ltd.		557816813	manufacture(59401-015)

Revised: 12/2019

Document Id: 9ab4d58d-2e8e-9859-e053-2995a90aa4e6

34390-5

Set id: 43e3a6e7-079f-46b8-9723-4c42fe36f9a7

Version: 2

Effective Time: 20191227

 

Imine Co., Ltd