Label: MYCOBACTER/MYCOPLASMA NOSODE 4009- mycobacter/mycoplasma nosode liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 63083-4009-2 - Packager: Professional Complementary Health Formulas
- 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 August 15, 2019
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ACTIVE INGREDIENTS
Arsenicum iodatum 30X
Sulphuricum acidum 30X
Nux vomica 100X
Sulphur 100X
and all the following at 30X, 60X, 100X:
Anthracinum
Mycobacterium abscessus
Mycobacterium avium-intracellulare
Mycobacterium chelonae
Mycobacterium fortuitum
Mycobacterium paratuberculosis
Mycoplasma arthritidis
Mycoplasma fermentans
Mycoplasma genitalium
Mycoplasma pneumoniae - QUESTIONS
- INDICATIONS
- PURPOSE
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WARNINGS
Severe or persistent symptoms may be a sign of a serious condition. Consult a doctor promptly if symptoms persist or are accompanied by a fever. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use.
- DIRECTIONS
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- LABEL
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INGREDIENTS AND APPEARANCE
MYCOBACTER/MYCOPLASMA NOSODE 4009
mycobacter/mycoplasma nosode liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63083-4009 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARSENIC TRIIODIDE (UNII: 3029988O2T) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIIODIDE 30 [hp_X] in 59 mL SULFURIC ACID (UNII: O40UQP6WCF) (SULFURIC ACID - UNII:O40UQP6WCF) SULFURIC ACID 30 [hp_X] in 59 mL STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 100 [hp_X] in 59 mL SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 100 [hp_X] in 59 mL BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N) (BACILLUS ANTHRACIS IMMUNOSERUM RABBIT - UNII:41LZ22DD4N) BACILLUS ANTHRACIS IMMUNOSERUM RABBIT 30 [hp_X] in 59 mL MYCOBACTERIUM ABSCESSUS (UNII: Y9O4JH3X21) (MYCOBACTERIUM ABSCESSUS - UNII:Y9O4JH3X21) MYCOBACTERIUM ABSCESSUS 30 [hp_X] in 59 mL MYCOBACTERIUM AVIUM (UNII: 67P4WI780Z) (MYCOBACTERIUM AVIUM - UNII:67P4WI780Z) MYCOBACTERIUM AVIUM 30 [hp_X] in 59 mL MYCOBACTERIUM AVIUM SUBSP. PARATUBERCULOSIS (UNII: XH0F4IP2RX) (MYCOBACTERIUM AVIUM SUBSP. PARATUBERCULOSIS - UNII:XH0F4IP2RX) MYCOBACTERIUM AVIUM SUBSP. PARATUBERCULOSIS 30 [hp_X] in 59 mL MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0) (MYCOPLASMA PNEUMONIAE - UNII:JQE470FAD0) MYCOPLASMA PNEUMONIAE 30 [hp_X] in 59 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63083-4009-2 59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 08/15/1985 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/15/1984 Labeler - Professional Complementary Health Formulas (167339027) Registrant - Natural Pharmaceutical Manufacturing LLC (015624923) Establishment Name Address ID/FEI Business Operations Natural Pharmaceutical Manufacturing LLC 015624923 manufacture(63083-4009)
