Label: LIMULUS NOURISHING- adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71464-0002-1 - 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
Mineral Oil
Hydrogenated Polydecene
Oleyl Alcohol
Stearic acid
Palmitic Acid
Glyceryl Stearate
PEG-100 Stearate
Beeswax
Cetyl Alcohol
Aronia Arbutifolia Fruit Extract
Glycerine
Butylene Glycol
Phenoxyethanol
Prunella Vulgaris Extract
Snail secretion filtrate
Phenoxyethanol
Vaccinium Macrocarpon (Cranberry) Fruit Extract
Euterpe Oleracea Fruit Extract
Vaccinium Angustifolium (Blueberry) Fruit Extract
Rubus Fruticosus (Blackberry) Fruit Extract
Rubus Idaeus (Raspberry) Fruit Extract
Triethanolamine
Phenoxyethanol
Fragrance
Chlorphenesin
Tetrasodium EDTA
Ceramide NP
Red Ginseng Extract - 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 NOURISHING
adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71464-0002 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 Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71464-0002-1 50 mL in 1 JAR; 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(71464-0002) Establishment Name Address ID/FEI Business Operations Skin R&D 694792365 label(71464-0002)
