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
IngredientStrength
ANTIMONY POTASSIUM TARTRATE6 [hp_C]/1
ANTIMONY TRISULFIDE6 [hp_C]/1
CHELIDONIUM MAJUS6 [hp_X]/1
FERROSOFERRIC PHOSPHATE6 [hp_X]/1
MARRUBIUM VULGARE9 [hp_C]/1
POTASSIUM CARBONATE30 [hp_C]/1
POTASSIUM CHLORIDE6 [hp_X]/1
POTASSIUM DICHROMATE12 [hp_X]/1
POTASSIUM SULFATE6 [hp_X]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiDL6OZ476V3, F79059A38U, 7E889U5RNN, 91GQH8I5F7, 7A72MUN24Z, BQN1B9B9HA, 660YQ98I10, T4423S18FM, 1K573LC5TV

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9e37788c-b1bf-42ae-aac9-b60601606144Product name820260122
95250459-30e4-45c1-b08a-993044f49109Product name220250805
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efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
1527ac37-808d-43be-a63e-74e1258dbe46Product name920250219
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362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5Product name820230322
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9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
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8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
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ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66096-706-23OHM Mucus Relief186 in 1 BOTTLETABLET, CHEWABLE1863

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66096-706OHM MUCUS RELIEF (ANTIMONIUM CRUDUM, ANTIMONIUM TARTARICUM, CHELIDONIUM MAJUS, FERRUM PHOSPHORICUM, KALI CARBOONICUM, KALI MURIATICUM, KALI SULPHURICUM, MARRUBIUM VULGARE.) TABLET, CHEWABLE [OHM PHARMA INC.]3Current NDC, Legacy NDC, 1 package rows20210112_f13bff50-7087-46dc-a958-b460a2af6283.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
66096-706-2366096070623186 TABLET, CHEWABLE in 1 BOTTLE (66096-706-23) 2015-05-140000-00-00NoNoCurrent