Label: LIMULUS THE 1 AND ONLY- niacinamide, adenosine lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 71464-0003-1 - 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 July 3, 2017
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water
Butylene Glycol
Cyclopentasiloxane
Dimethicone
Dimethicone/PEG-10/15 Crosspolymer
Dipropylene Glycol
Sodium Citrate
Tocopherol
Sea Water
Butylene Glycol
Dimethicone
Niacinamide
Sodium Chloride
Galactomyces Ferment Filtrate
Panax Ginseng Callus Extract
Glycerin
1,2-Hexanediol
Prunella Vulgaris Extract
Hamamelis Virginiana (Witch Hazel) Water
Propylene Glycol
Centella Asiatica (Centella) Extract
Portulaca Oleracea Extract
Phenoxyethanol
Aloe Barbadensis Leaf Juice
Hydrolyzed Collagen
Phenoxyethanol
Cetyl PEG/PPG-10/1 Dimethicone
Chlorphenesin
Allantoin
Fragrance
Panthenol
Adenosine
Disodium EDTA
Sodium Hyaluronate - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
Precautions for Use
1. Consult with a medical specialist if any abnormal symptoms or side effects, such as red spots, swelling, or itching, occur during the use of this product.
2. Do not use the product on wounded areas.
3. Precautions for storage and handling
1) Keep out of reach of children.
2) Store away from direct sunlight.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LIMULUS THE 1 AND ONLY
niacinamide, adenosine lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71464-0003 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 mL NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 2 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71464-0003-1 100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/01/2017 Labeler - Skin R&D (694792365) Registrant - Skin R&D (694792365) Establishment Name Address ID/FEI Business Operations Daegu Haany University 690282954 manufacture(71464-0003) Establishment Name Address ID/FEI Business Operations Skin R&D 694792365 label(71464-0003)
