Label: CLARA- psyllium husk granule
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Contains inactivated NDC Code(s)
NDC Code(s): 76369-1001-1 - Packager: Handock Cosmetics Inc
- Category: HUMAN OTC DRUG LABEL
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 August 26, 2011
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
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PURPOSE
■ Enhances Liver function, detoxification and anti-inflammatory effects
■ Intestinal toxic emissions and health
■ Removes constipation and bad breadth
■ Dietary Fiber warranty
■ Enhances blood pressure and immune system
■ Diabetes prevention
■ Reduces Cholesterol
■ Prevention of adult diseases and osteoporosis
■ Removes Gastrointestinal Disorders and stomach gas
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
■ If you are pregnant, nursing, taking any medications or planning any medical procedure, consult your doctor before
use. Discontinue use and consult your doctor if any adverse reactions occur.
■ Please check the ingredients before taking if there are allergic or idiosyncratic symptoms
■ Do not take if the product of expiration date is expired
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLARA
psyllium husk granuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76369-1001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PSYLLIUM HUSK (UNII: 0SHO53407G) (PSYLLIUM HUSK - UNII:0SHO53407G) PSYLLIUM HUSK 3.25 g in 5 g Inactive Ingredients Ingredient Name Strength INULIN (UNII: JOS53KRJ01) MALTODEXTRIN (UNII: 7CVR7L4A2D) KELP BASS (UNII: 24ZZ99M3KV) lactulose (UNII: 9U7D5QH5AE) RICE (UNII: 659G217HPG) TEA LEAF (UNII: GH42T47V24) CYSTINE (UNII: 48TCX9A1VT) PROPOLIS WAX (UNII: 6Y8XYV2NOF) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76369-1001-1 5 g in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/26/2011 Labeler - Handock Cosmetics Inc (688037204) Registrant - Handock Cosmetics Inc (688037204) Establishment Name Address ID/FEI Business Operations Handock Cosmetics Inc 688037204 manufacture