CAUSTICUM

Manufacturer
SEVENE USA
Effective date
2025-02-10
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:31:58

Label at a glance#

ProductCAUSTICUM 200ck
Active ingredientCAUSTICUM
Label structure12 sections

Dosage and administration

(adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

Storage and handling

Store at room temperature.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

CAUSTICUM 200ck

TRADITIONALLY USED FOR:

OTC - PURPOSE SECTION

URINARY INCONTINENCE

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

(adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

USE

INDICATIONS & USAGE SECTION

TRADITIONALLY USED FOR: URINARY INCONTINENCE*

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.

WARNINGS

WARNINGS SECTION

Stop use and ask a physician if symptoms persist for more than 3 days or worsen.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

In case of overdoes, get medical help.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

Store at room temperature.

OTC - DO NOT USE SECTION

Do not use if tamper-evidence seal is broken.

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

ORGANIC SUCROSE

ORGANIC VERIFIED BY ALPES CONTROLE 2021/A03M216K/1.

QUESTIONS OR COMMENTS?

OTC - QUESTIONS SECTION

EMAIL: INFO@OLLOIS.COM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CAUSTICUM 200CKCAUSTICUM 200CK

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76472-4072-1CAUSTICUM200ck80 in 1 CYLINDERPELLET804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76472-4072CAUSTICUM 200CK (CAUSTICUM) PELLET [SEVENE USA]4Current NDC, Legacy NDC, 1 package rows20250212_ed9b814b-eca0-f1bd-e053-2a95a90a082f.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76472-407276472-4072-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554IACT
CAUSTICUMDD5FO1WKFUACTIB

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
CAUSTICUM 200ckCAUSTICUMSEVENE USAed9b814b-eca0-f1bd-e053-2a95a90a082f2025-02-10WarningsExact identifier
ndc (package): 76472-4072-1
ndc (product): 76472-4072
ndc11 (package): 76472407201
spl id: 2dcc77bf-dfbe-3a63-e063-6394a90ad999
spl set id: ed9b814b-eca0-f1bd-e053-2a95a90a082f

Reported adverse events (FAERS/openFDA)#

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