FDA.reportPublic FDA data

Cold

Product NDC
66096-114
11-digit product format
660960114
Labeler code
66096
Product ID
66096-114_d44b7dc6-41ea-5d79-e053-2995a90a5919
Type
HUMAN OTC DRUG
Nonproprietary name
Aconitum Napellus, Bryonia Alba, Eupatorium Perfoliatum, Ferrum Phosphoricum, Gelsemium Sempervirens, Kali Bichromicum, Kali lodatum, Zincum Gluconicum.
Dosage form
LIQUID
Route
ORAL
Labeler
OHM PHARMA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2017-01-09
Substance
ACONITUM NAPELLUS; BRYONIA ALBA ROOT; EUPATORIUM PERFOLIATUM FLOWERING TOP; FERROSOFERRIC PHOSPHATE; GELSEMIUM SEMPERVIRENS ROOT; POTASSIUM DICHROMATE; POTASSIUM IODIDE; ZINC GLUCONATE
Active strength
4; 6; 4; 4; 6; 6; 6; 3 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes
Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Cold
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACONITUM NAPELLUS4 [hp_X]/59mL
BRYONIA ALBA ROOT6 [hp_X]/59mL
EUPATORIUM PERFOLIATUM FLOWERING TOP4 [hp_X]/59mL
FERROSOFERRIC PHOSPHATE4 [hp_X]/59mL
GELSEMIUM SEMPERVIRENS ROOT6 [hp_X]/59mL
POTASSIUM DICHROMATE6 [hp_X]/59mL
POTASSIUM IODIDE6 [hp_X]/59mL
ZINC GLUCONATE3 [hp_X]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 8 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
U0NQ8555JDInternal UNII lookup
T7J046YI2BInternal UNII lookup
1W0775VX6EInternal UNII lookup
91GQH8I5F7Internal UNII lookup
639KR60Q1QInternal UNII lookup
T4423S18FMInternal UNII lookup
1C4QK22F9JInternal UNII lookup
U6WSN5SQ1ZInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
12c71753-bed4-4f0c-970e-8564b2dd2e2eAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66096-114-05Cold59 mL in 1 BOTTLE, SPRAYLIQUID595

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66096-114COLD (ACONITUM NAPELLUS, BRYONIA ALBA, EUPATORIUM PERFOLIATUM, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, KALI BICHROMICUM, KALI LODATUM, ZINCUM GLUCONICUM.) LIQUID [OHM PHARMA INC.]5Current NDC, Legacy NDC, 1 package rows20211230_12c71753-bed4-4f0c-970e-8564b2dd2e2e.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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ColdACONITUM NAPELLUS, BRYONIA ALBA, EUPATORIUM PERFOLIATUM, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, KALI BICHROMICUM, KALI LODATUM, ZINCUM GLUCONICUM.OHM PHARMA INC.12c71753-bed4-4f0c-970e-8564b2dd2e2e2021-12-29WarningsExact identifier
ndc (product): 66096-114

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66096-114-056609601140559 mL in 1 BOTTLE, SPRAY (66096-114-05) 59 ml2017-01-090000-00-00NoNoCurrent