Label: LIMULUS BIO CELLULOSE MASK- glycerin, niacinamide, adenosine kit
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Contains inactivated NDC Code(s)
NDC Code(s): 71464-0004-1, 71464-0005-1, 71464-0006-1, 71464-0007-1 - Packager: Skin R&D
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated June 28, 2017
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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INDICATIONS & USAGE
- Open the package and unfold the cellulose mask pack. Then, remove the white film.
- Attach the product tightly on your face using the side where the white film was removed. Then, remove the fabric on the other side.
- Carefully adjust the position of the mask on your face. Try not to damage the soft cellulose mask pack.
- After taking 20-30 minutes of rest, remove the mask. Let your skin absorb the remaining essence with gently dabbing motion.
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WARNINGS
1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children - DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LIMULUS BIO CELLULOSE MASK
glycerin, niacinamide, adenosine kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71464-0004 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71464-0004-1 1 in 1 PACKAGE; Type 0: Not a Combination Product 06/28/2017 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 POUCH 28 g Part 2 1 POUCH 28 g Part 3 1 POUCH 28 g Part 1 of 3 LIMULUS BIO CELLULOSE MASK WRINKLE CARE
adenosine liquidProduct Information Item Code (Source) NDC:71464-0005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71464-0005-1 28 g in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/28/2017 Part 2 of 3 LIMULUS BIO CELLULOSE MASK WHITENING
niacinamide liquidProduct Information Item Code (Source) NDC:71464-0006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 2 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71464-0006-1 28 g in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/28/2017 Part 3 of 3 LIMULUS BIO CELLULOSE MASK AC CARE
glycerin liquidProduct Information Item Code (Source) NDC:71464-0007 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 16 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71464-0007-1 28 g in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part347 06/28/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/28/2017 Labeler - Skin R&D (694792365) Registrant - Skin R&D (694792365) Establishment Name Address ID/FEI Business Operations SLC CO.,LTD. 694477505 manufacture(71464-0005, 71464-0004, 71464-0006, 71464-0007) Establishment Name Address ID/FEI Business Operations Skin R&D 694792365 label(71464-0004, 71464-0005, 71464-0006, 71464-0007)
