FDA.reportPublic FDA data

Spongilla lacustris MT

Manufacturer
OHM PHARMA INC.
Effective date
2021-12-29
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:15:26

Label at a glance#

ProductSpongilla lacustris MT
Active ingredientSPONGILLA LACUSTRIS
Label structure5 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Spongilla Lacustris

WARNINGS SECTION

Caution: for manufacturing,

processing or repacking only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

INACTIVE INGREDIENT SECTION

Inactive Ingredient: Ethanol 64%, Purified Water

OTC - QUESTIONS SECTION

Distributed by: OHM Pharma

Mineral Wells, TX 76067

www.ohmpharma.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

​NDC 66096-749-08

ohm

PHARMA

Spongilla lacustris MT

0.250

Caution: for manufacturing,

processing or repacking only.

Batch no. 38798

Retest Date: 11/2021

Active Ingredient: Spongilla Lacustris

Inactive Ingredient: Ethanol 64%, Purified Water

Distributed by: OHM Pharma

Mineral Wells, TX 76067

www.ohmpharma.com

Spongilla lacustris MTSpongilla lacustris MT

OTC - PURPOSE SECTION

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66096-749-08Spongilla lacustris MT0.25 L in 1 BOTTLETINCTURE0.253

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66096-749SPONGILLA LACUSTRIS MT (SPONGILLA LACUSTRIS) TINCTURE [OHM PHARMA INC.]3Current NDC, Legacy NDC, 1 package rows20211230_a855d4ca-52ed-4e69-93b5-7304bcc84f73.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66096-74966096-749-08

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
SPONGILLA LACUSTRIS6SZ0G98BHMACTIB

Source Document#

Source XML

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
Spongilla lacustris MTSPONGILLA LACUSTRISOHM PHARMA INC.a855d4ca-52ed-4e69-93b5-7304bcc84f732021-12-29WarningsExact identifier
ndc (package): 66096-749-08
ndc (product): 66096-749
ndc11 (package): 66096074908
spl id: d449d3d9-49bd-2a4b-e053-2995a90a5a95
spl set id: a855d4ca-52ed-4e69-93b5-7304bcc84f73

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.