Label: CRANBERRY RELIEF- urinary support powder
- NDC Code(s): 27135-0356-1
- Packager: The Garmon Corporation
- Category: OTC ANIMAL DRUG LABEL
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Drug Label Information
Updated November 11, 2013
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PRECAUTIONS
- PURPOSE
- DOSAGE & ADMINISTRATION
- WARNINGS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CRANBERRY RELIEF
urinary support powderProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:27135-0356 Route of Administration Oral Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CRANBERRY (UNII: 0MVO31Q3QS) (CRANBERRY - UNII:0MVO31Q3QS) CRANBERRY 210 mg ECHINACEA PURPUREA (UNII: QI7G114Y98) (ECHINACEA PURPUREA - UNII:QI7G114Y98) ECHINACEA PURPUREA 105 mg CALCIUM ASCORBATE (UNII: 183E4W213W) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID 34 mg MAHONIA AQUIFOLIUM ROOT BARK (UNII: VZJ9F3C3SB) (MAHONIA AQUIFOLIUM ROOT BARK - UNII:VZJ9F3C3SB) MAHONIA AQUIFOLIUM ROOT BARK 34 mg Inactive Ingredients Ingredient Name Strength STEVIA LEAF (UNII: 6TC6NN0876) COW MILK (UNII: 917J3173FT) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color brown Score Shape Size Flavor CRANBERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:27135-0356-1 90 in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/01/1996 Labeler - The Garmon Corporation (011706236) Registrant - The Garmon Corporation (011706236) Establishment Name Address ID/FEI Business Operations The Garmon Corporation 011706236 manufacture, api manufacture