Label: TESTOSTERONE tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 44117-0001-1 - Packager: Zoe Processing
- 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 April 3, 2013
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- INDICATIONS
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WARNINGS
Not intended for persons under the age of 18. If pregnant or breast-feeding, do not use. Consult a health professional prior to use if you ahve any pre-existing medical conditions or take any prescription medications. Do not consume with any caffeine or stimulants. Improper use will not improve results and is potentially hazardous to a person's health. Use only as directed.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. To report a serious adverse event or obtain product information, please call 1-866-607-2768
- DIRECTIONS
- INACTIVE INGREDIENTS
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS AND USAGE
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
TESTOSTERONE
testosterone tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44117-0001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TESTOSTERONE (UNII: 3XMK78S47O) (TESTOSTERONE - UNII:3XMK78S47O) TESTOSTERONE 30 [hp_X] in 1 mg Inactive Ingredients Ingredient Name Strength CREATINE MONOHYDRATE (UNII: 9603LN7R2Q) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color white Score no score Shape ROUND (oblong) Size 23mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:44117-0001-1 67600 mg in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/03/2013 Labeler - Zoe Processing (040866348) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(44117-0001)