Label: TYPE 7 STRESS ANXIETY REGULAR- kali phosphoricum, phosphoricum acidum, sepia, sulphur, calcarea carbonica, silicea tablet, orally disintegrating
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Contains inactivated NDC Code(s)
NDC Code(s): 50169-0004-1 - Packager: T-Gone Remedies
- 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 24, 2013
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- ACTIVE INGREDIENTS
- INDICATIONS
- WARNINGS
- DIRECTIONS
- INACTIVE INGREDIENTS
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS AND USAGE
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
TYPE 7 STRESS ANXIETY REGULAR
kali phosphoricum, phosphoricum acidum, sepia, sulphur, calcarea carbonica, silicea tablet, orally disintegratingProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50169-0004 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR) POTASSIUM PHOSPHATE, DIBASIC 3 [hp_X] in 1 mg PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID 6 [hp_X] in 1 mg SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2) SEPIA OFFICINALIS JUICE 6 [hp_X] in 1 mg SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 6 [hp_X] in 1 mg OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X] in 1 mg SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (COLLOIDAL SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 12 [hp_X] in 1 mg Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) Product Characteristics Color white Score no score Shape ROUND (convex) Size 6mm Flavor Imprint Code Diamond Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50169-0004-1 15000 mg in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/24/2013 Labeler - T-Gone Remedies (846965817) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(50169-0004)