Label: MEDIFENSE CLEAN HAND SERUM GREENERY BOUQUET- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 74005-060-01 - Packager: L&P Cosmetic Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 19, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
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Warnings
For external use only. Flammable. Keep away from heat or flame
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Do not use
• in children less than 2 months of age
• on open skin wounds
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition. - Keep out of reach of children
- Uses
- Directions
- Other information
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Inactive ingredients
1,2-Hexanediol, 3-O-Ethyl Ascorbic Acid, Acrylates Copolymer, Aminomethyl Propanol, Benzyl Salicylate, Butylphenyl Methylpropional, Caprylic/Capric Triglyceride, Carbomer, Cetyl Alcohol, Chamomilla Recutita (Matricaria) Flower Extract, Citric acid, Cymbopogon Schoenanthus Extract, Eugenol, Fragrance, Glycerin, Lavandula Angustifolia (Lavender) Flower Extract, Linalool, Olea Europaea (Olive) Fruit Oil, Panthenol, Rosmarinus Officinalis (Rosemary) Extract, Saccharide Isomerate, Salvia Officinalis (Sage) Leaf Extract, Sodium Citrate, Sodium Hyaluronate, Styrene/Acrylates Copolymer, Tocopheryl Acetate, Water
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MEDIFENSE CLEAN HAND SERUM GREENERY BOUQUET
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74005-060 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 31 mL in 50 mL Inactive Ingredients Ingredient Name Strength 1,2-Hexanediol (UNII: TR046Y3K1G) 3-O-Ethyl Ascorbic Acid (UNII: 6MW60CB71P) BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E) AminomethylPropanol (UNII: LU49E6626Q) Benzyl Salicylate (UNII: WAO5MNK9TU) Butylphenyl Methylpropional (UNII: T7540GJV69) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) Cetyl Alcohol (UNII: 936JST6JCN) CHAMOMILE (UNII: FGL3685T2X) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CYMBOPOGON SCHOENANTHUS TOP (UNII: 9SJI1LW39W) Eugenol (UNII: 3T8H1794QW) Glycerin (UNII: PDC6A3C0OX) LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M) LINALOOL, (+/-)- (UNII: D81QY6I88E) OLIVE OIL (UNII: 6UYK2W1W1E) Panthenol (UNII: WV9CM0O67Z) ROSEMARY (UNII: IJ67X351P9) Saccharide Isomerate (UNII: W8K377W98I) Sage (UNII: 065C5D077J) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) HYALURONATE SODIUM (UNII: YSE9PPT4TH) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74005-060-01 50 mL in 1 CONTAINER; Type 0: Not a Combination Product 11/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 11/01/2020 Labeler - L&P Cosmetic Co., Ltd. (557821713) Registrant - L&P Cosmetic Co., Ltd. (557821713) Establishment Name Address ID/FEI Business Operations E.CIS COSMETIC.,Co.Ltd 689846270 manufacture(74005-060)
