Label: METX solution/ drops
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Contains inactivated NDC Code(s)
NDC Code(s): 61727-001-00 - Packager: Homeocare Laboratories Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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 7, 2016
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- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- QUESTIONS
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
METX
metx solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61727-001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (THYROID, UNSPECIFIED - UNII:0B4FDL9I6P) THYROID, UNSPECIFIED 4 [hp_C] in 60 mL FUCUS SERRATUS (UNII: V8K40WNW5B) (FUCUS SERRATUS - UNII:V8K40WNW5B) FUCUS SERRATUS 1 [hp_C] in 60 mL TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION 6 [hp_C] in 60 mL GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE 6 [hp_C] in 60 mL SODIUM SULFIDE (UNII: YGR27ZW0Y7) (SULFIDE ION - UNII:G15I91XETI) SODIUM SULFIDE 6 [hp_C] in 60 mL LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE 3 [hp_C] in 60 mL SUS SCROFA PLACENTA (UNII: C8CV8867O8) (SUS SCROFA PLACENTA - UNII:C8CV8867O8) SUS SCROFA PLACENTA 30 [hp_C] in 60 mL ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U) ANTIMONY TRISULFIDE 5 [hp_C] in 60 mL BOS TAURUS HYPOTHALAMUS (UNII: S6G2NLH4Y7) (BOS TAURUS HYPOTHALAMUS - UNII:S6G2NLH4Y7) BOS TAURUS HYPOTHALAMUS 7 [hp_C] in 60 mL Inactive Ingredients Ingredient Name Strength 1-(4-CHLOROPHENYL)-1-PHENYLETHANOL (UNII: 6149LO684B) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61727-001-00 1 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 01/20/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/20/2016 Labeler - Homeocare Laboratories Inc. (088248828) Establishment Name Address ID/FEI Business Operations HomeoCare Laboratories Inc. 088248828 manufacture(61727-001)