SULPHUR

Manufacturer: SEVENE USA
Effective date: 2025-02-11
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 02:32:03

Label at a glance#

ProductSULPHUR 200ck

Active ingredientSULFUR

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 physician.

Contacts and useful links#

Websitewww.ollois.com

www.ollois.com

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

HOMEOPATHIC DILUTION OF HPUS SULPHUR 200ck **C,K, CK, AND X ARE HOMEOPATHIC DILUTIONS.

TRADITIONALLY USED FOR

OTC - PURPOSE SECTION

Stinging edemas from stings or allergies, relieved by cold*

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 physician.

USE

INDICATIONS & USAGE SECTION

Condition listed above or as directed by a physician.

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.

OTHER INFORMATION

OTHER SAFETY INFORMATION

Store at room temperature.

OTC - DO NOT USE SECTION

Do not use if pellet-dispenser seal is broken.

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Sucrose.

QUESTIONS?

OTC - QUESTIONS SECTION

INFO@OLLOIS.COM * www.ollois.com * MADE IN FRANCE. NOT REVIEWED BY THE FDA AND NOT GUARANTEED TO BE EFFECTIVE. THIS HOMEOPATHIC DILUTION MAY NOT BE SUSCEPTIBLE TO SCIENTIFIC MEASUREMENT.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76472-3037-1	2025-02-11	C162847	48780-1	2cef2736-5bde-d83d-e063-dadaa90ab31f	Sevene USA (as PLD) - SULPHUR 200ck (76472-3037)
76472-3037-1	2025-01-30	C162847	48780-1	2cef2736-5bde-d83d-e063-dadaa90ab31f	Sevene USA (as PLD) - SULPHUR 200ck (76472-3037)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76472-3037-1	SULPHUR200ck	80 in 1 CYLINDER	PELLET	80		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76472-3037	SULPHUR 200CK (SULPHUR) PELLET [SEVENE USA]	4	Current NDC, Legacy NDC, 1 package rows	20250213_cf8a0d33-999d-6860-e053-2995a90af8c6.zip

Products#

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

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

SULPHUR 200ck
SULPHUR
SUCROSE
SULFUR

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76472-3037	76472-3037-1

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
Name	UNII	Kind
SUCROSE	C151H8M554	IACT
SULFUR	70FD1KFU70	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SULPHUR 200ck	SULPHUR	SEVENE USA	cf8a0d33-999d-6860-e053-2995a90af8c6	2025-02-11	Warnings	Exact identifier ndc (package): 76472-3037-1 ndc (product): 76472-3037 ndc11 (package): 76472303701 spl id: 2ddc7745-9549-8289-e063-6294a90a1a77 spl set id: cf8a0d33-999d-6860-e053-2995a90af8c6

Reported adverse events (FAERS/openFDA)#

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