Home NDC 66096-706 OHM Mucus Relief
Product NDC 66096-706
11-digit product format 660960706
Labeler code 66096
Product ID 66096-706_b8a719c7-3b71-773b-e053-2995a90af29b
Type HUMAN OTC DRUG
Nonproprietary name Antimonium Crudum, Antimonium Tartaricum, Chelidonium Majus, Ferrum Phosphoricum, Kali Carboonicum, Kali muriaticum, Kali Sulphuricum, Marrubium Vulgare.
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler OHM PHARMA INC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-05-14
Substance ANTIMONY POTASSIUM TARTRATE; ANTIMONY TRISULFIDE; CHELIDONIUM MAJUS; FERROSOFERRIC PHOSPHATE; MARRUBIUM VULGARE; POTASSIUM CARBONATE; POTASSIUM CHLORIDE; POTASSIUM DICHROMATE; POTASSIUM SULFATE
Active strength 6; 6; 6; 6; 9; 30; 6; 12; 6 [hp_C]/1; [hp_C]/1; [hp_X]/1; [hp_X]/1; [hp_C]/1; [hp_C]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Compounds [CS], Potassium Salt [EPC], Potassium Salt [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base OHM Mucus Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ANTIMONY TRISULFIDE 6 [hp_C]/1 ANTIMONY POTASSIUM TARTRATE 6 [hp_C]/1 CHELIDONIUM MAJUS 6 [hp_X]/1 FERROSOFERRIC PHOSPHATE 6 [hp_X]/1 POTASSIUM DICHROMATE 9 [hp_C]/1 POTASSIUM CARBONATE 30 [hp_C]/1 POTASSIUM CHLORIDE 6 [hp_X]/1 POTASSIUM SULFATE 12 [hp_X]/1 MARRUBIUM VULGARE 6 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 9 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 66096-706-23 OHM Mucus Relief 186 in 1 BOTTLE TABLET, CHEWABLE 186 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 66096-706 OHM MUCUS RELIEF (ANTIMONIUM CRUDUM, ANTIMONIUM TARTARICUM, CHELIDONIUM MAJUS, FERRUM PHOSPHORICUM, KALI CARBOONICUM, KALI MURIATICUM, KALI SULPHURICUM, MARRUBIUM VULGARE.) TABLET, CHEWABLE [OHM PHARMA INC.] 3 Current NDC, Legacy NDC, 1 package rows 20210112_f13bff50-7087-46dc-a958-b460a2af6283.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join OHM Mucus Relief ANTIMONIUM CRUDUM, ANTIMONIUM TARTARICUM, CHELIDONIUM MAJUS, FERRUM PHOSPHORICUM, KALI CARBOONICUM, KALI MURIATICUM, KALI SULPHURICUM, MARRUBIUM VULGARE. OHM PHARMA INC. f13bff50-7087-46dc-a958-b460a2af6283 2021-01-11 Warnings Exact identifier ndc (product): 66096-706
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 66096-706-23 66096070623 186 TABLET, CHEWABLE in 1 BOTTLE (66096-706-23) 2015-05-14 0000-00-00 No No Current