Label: PLEO ZINC- zinc gluconate solution/ drops
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Contains inactivated NDC Code(s)
NDC Code(s): 60681-5502-1 - Packager: Sanum Kehlbeck GmbH & Co. KG
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated March 6, 2013
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- SPL UNCLASSIFIED SECTION
- Indications
- INACTIVE INGREDIENT
- Tamper Evident
- DOSAGE
- WARNING
- STORAGE AND HANDLING
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton
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INGREDIENTS AND APPEARANCE
PLEO ZINC
zinc gluconate solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-5502 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength zinc gluconate (UNII: U6WSN5SQ1Z) (zinc cation - UNII:13S1S8SF37) zinc gluconate 3 [hp_X] in 30 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) alcohol (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60681-5502-1 1 in 1 CARTON 1 30 mL in 1 BOTTLE, DROPPER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved homeopathic 06/15/2010 Labeler - Sanum Kehlbeck GmbH & Co. KG (318386133) Establishment Name Address ID/FEI Business Operations SANUM KEHLBECK GmbH & Co. KG 318386133 MANUFACTURE(60681-5502)