Label: HES CLEAN PLUS- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 42979-110-01 - Packager: DOCTOR C&C CO., LTD.
- Category: HUMAN OTC DRUG LABEL
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 February 25, 2013
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
WATER, DISODIUM LAURETH SULFOSUCCINATE, Acrylates Copolymer, Cocamidopropyl Betaine, Decyl Glucoside, Sophora Angustifolia Root Extract, Hippophae Rhamnoides Extract, Lactuca Indica Extract, Corydalis Ochotensis Extract, Draba Nemorosa Extract, Chenopodium Album Flower Extract, Lactobacillus/Soybean Extract Ferment Filtrate, Salix Alba (Willow) Bark Extract, Cinnamomum Cassia Bark Extract, Origanum Vulgare Leaf Extract, Chamaecyparis Obtusa Leaf Extract, Portulaca Oleracea Extract, Scutellaria Baicalensis Root Extract, Rosemarinus Officinalis (Rosemary) Leaf Extract, Lavandula Angustifolia Extract, Octimum Basilicum (Basil) Extract, Althaea Officinalis Extract, Houttuynia Cordata Extract, Chamomilla Reacutita Flower Extract, Foeniculum Vulgare (Fennl) Extract, Pyrus Malus (Apple) Fruit Water, Propylene Glycol, Ethanol, PEG-40 Hydrogenated Castor Oil - PURPOSE
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WARNINGS
Warnings:
1. For external use only.
2. Do not use on wounds or other infected areas.
3. Stop use if any of the following symptoms appear and consult a doctor if they persist.
- Redness, swelling, itchiness, irritation, rash, etc.
- Any of the above symptoms when exposed to direct sunlight.
4. Persists consult your doctor or pharmacist. - KEEP OUT OF REACH OF CHILDREN
- DOSAGE AND ADMINISTRATION
- INDICATIONS AND USAGE
- PACKAGE LABEL. PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HES CLEAN PLUS
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:42979-110 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 4 mg in 50 mL Inactive Ingredients Ingredient Name Strength DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E) WATER (UNII: 059QF0KO0R) SALIX ALBA BARK (UNII: 205MXS71H7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42979-110-01 50 mL in 1 CARTON Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 10/01/2012 Labeler - DOCTOR C&C CO., LTD. (557816136) Registrant - DOCTOR C&C CO., LTD. (557816136) Establishment Name Address ID/FEI Business Operations DOCTOR C&C CO., LTD. 557816136 manufacture(42979-110)