Label: OHM MUCUS RELIEF- antimonium crudum, antimonium tartaricum, chelidonium majus, ferrum phosphoricum, kali carboonicum, kali muriaticum, kali sulphuricum, marrubium vulgare. tablet, chewable
- NDC Code(s): 66096-706-23
- Packager: OHM PHARMA 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 January 11, 2021
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ACTIVE INGREDIENT
ACTIVE INGREDIENTS (HPUS*): Each tablet contains equal parts of: Antimonium Crudum 6C, Antimonium Tartaricum 6C, Chelidonium Majus 6X, Ferrum Phosphoricum 6X, Kali Carboonicum 30C, Kali Muriaticum 6X, Kali Sulphuricum 6X, Marrubium Vulgare 9C.
* *The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United States.
- INDICATIONS & USAGE
- WARNINGS
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DOSAGE & ADMINISTRATION
DIRECTIONS: Chew or dissolve tablets under tongue at least 30 minutes away from food. Adults and children 12+: First dose: Take 2 tablets every 20 minutes or until symptoms improve. Daily: Take 2 tablets 3 times a day. Children 3-12 years: First dose: Take 1 tablet every 20 minutes or until symptoms improve. Daily: Take 1 tablet 3 times a day. Can be crushed and sprinkled under tongue.
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
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INGREDIENTS AND APPEARANCE
OHM MUCUS RELIEF
antimonium crudum, antimonium tartaricum, chelidonium majus, ferrum phosphoricum, kali carboonicum, kali muriaticum, kali sulphuricum, marrubium vulgare. tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66096-706 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U) ANTIMONY TRISULFIDE 6 [hp_C] ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY POTASSIUM TARTRATE 6 [hp_C] CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (CHELIDONIUM MAJUS - UNII:7E889U5RNN) CHELIDONIUM MAJUS 6 [hp_X] FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7) FERROSOFERRIC PHOSPHATE 6 [hp_X] POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE 12 [hp_X] POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE 30 [hp_C] POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CATION 6 [hp_X] POTASSIUM SULFATE (UNII: 1K573LC5TV) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM SULFATE 6 [hp_X] MARRUBIUM VULGARE (UNII: 7A72MUN24Z) (MARRUBIUM VULGARE - UNII:7A72MUN24Z) MARRUBIUM VULGARE 9 [hp_C] Inactive Ingredients Ingredient Name Strength DEXTROSE (UNII: IY9XDZ35W2) MAGNESIUM STEARATE (UNII: 70097M6I30) Product Characteristics Color white Score no score Shape ROUND Size 6mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66096-706-23 186 in 1 BOTTLE; Type 0: Not a Combination Product 05/14/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/14/2015 Labeler - OHM PHARMA INC. (030572478) Registrant - OHM PHARMA INC. (030572478) Establishment Name Address ID/FEI Business Operations OHM PHARMA INC. 030572478 manufacture(66096-706)
