Sallys Box Loverecipe Paprika Mask by Imine Co., Ltd 59401-009_Deactivation

Sallys Box Loverecipe Paprika Mask by

Drug Labeling and Warnings

Sallys Box Loverecipe Paprika 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 LOVERECIPE PAPRIKA 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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59401-009_Deactivation

Allantoin (0.02%)

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. Take the product out of the package and adhere it evenly over your face avoiding the eye and mouth area. 3. Remove it after 10-20 minutes. Using your fingers, gently pat any remaining product into the skin until thoroughly absorbed.

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, Butylene Glycol, Glycerin, Citrus Paradisi (Grapefruit) Fruit Extract, Alcohol, Xanthan Gum, PEG-60 Hydrogenated Castor Oil, Capsicum Annuum Fruit Extract, Ethylhexylglycerin, Panthenol, Arnica Montana Flower Extract, Artemisia Absinthium Extract, Achillea Millefolium Extract, Gentiana Lutea Root Extract, Sodium Hyaluronate, Disodium EDTA, Phenoxyethanol, Fragrance

SALLYS BOX LOVERECIPE PAPRIKA MASK 
allantoin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59401-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.004 mg  in 20 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCERIN (UNII: PDC6A3C0OX)
GRAPEFRUIT (UNII: O82C39RR8C)
ALCOHOL (UNII: 3K9958V90M)
XANTHAN GUM (UNII: TTV12P4NEE)
PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
PAPRIKA (UNII: X72Z47861V)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PANTHENOL (UNII: WV9CM0O67Z)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
WORMWOOD (UNII: F84709P2XV)
ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
GENTIANA LUTEA ROOT (UNII: S72O3284MS)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59401-009-01	20 mL in 1 POUCH; Type 0: Not a Combination Product	11/18/2014	12/26/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/18/2014	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(59401-009)

Revised: 12/2019

Document Id: 9aa43e26-1e61-2e34-e053-2995a90a398a

34390-5

Set id: d5dc53c0-5ec0-4498-8229-9401626ccb67

Version: 2

Effective Time: 20191226

 

Imine Co., Ltd