NDC | 50169-0007-1 |
Set ID | 56716884-75fa-43a8-9194-d5426bfbd651 |
Category | HUMAN OTC DRUG LABEL |
Packager | TGone Remedies Ltd |
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Product Class | |
Product Number | |
Application Number |
- ACTIVE INGREDIENTS:
- INDICATIONS:
- WARNINGS:
- KEEP OUT OF THE REACH OF CHILDREN:
- DIRECTIONS:
- INDICATIONS:
- INACTIVE INGREDIENTS:
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QUESTIONS:
Manufactured for:
T-Gone Remedies
375 N. Stephanie St., Ste 1411
Henderson, NV 89014-8909
Web: www.t-gone.com
Tel: 800-314-2910
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
TYPE 7 STRESS ANXIETY MAX
calcarea carbonica, kali phosphoricum, phosphoricum acidum, sepia, silicea, sulphur tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50169-0007 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 200 [hp_C] in 1 mg POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR) POTASSIUM PHOSPHATE, DIBASIC 200 [hp_C] in 1 mg PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID 200 [hp_C] in 1 mg SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2) SEPIA OFFICINALIS JUICE 200 [hp_C] in 1 mg SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (COLLOIDAL SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 200 [hp_C] in 1 mg SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 200 [hp_C] 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:50169-0007-1 15000 mg in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/08/2014 Labeler - TGone Remedies Ltd (846965817) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(50169-0007) , api manufacture(50169-0007) , label(50169-0007) , pack(50169-0007)