SULPHUR

Manufacturer: Remedy Makers
Effective date: 2010-03-12
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:02:13

Label at a glance#

ProductSULPHUR

Active ingredientSULFUR

Label structure2 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Free from yeast, wheat, corn, and soy.
DIRECTIONS: Dissolve 3 or 4 pellets
in mouth or under tongue 3 times a day or as directed by a physician.
Children 2 years and older take 1/2
adult dose.
INDICATIONS: To be used according
to standard homeopathic indications
for self limiting conditions such as
those indicated on the front panel or as directed by a physician.
Warnings: *Use only if cap and
seal are unbroken. * Keep this and all medications out of reach of children.
* If symptoms persist for more then 3
days, consult your physician.
*As with any drug, if your are pregnant or nursing a baby, seek the advice of a
health professional before using this product.*Store tightly closed in a cool, dark place.
Made according to The Homeopathic Pharmacopoeia of the United States by: Remedy Makers, Pomona, CA 91768

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SULPHUR 6C

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0310191158528	GTIN-13: 0310191158528 EAN-13: 0310191158528 GTIN-12: 310191158528 UPC-A: 310191158528 GTIN storage (14 digits): 00310191158528	2e7a9203-1fb9-429f-86af-5d6e83794603.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
10191-1585-2	2019-10-21	C162847	48780-1	956f9ecf-cbc7-621f-e053-dbdaa90a74ad	SULPHUR 6C (Sulfur)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10191-1585-2	SULPHUR	151 in 1 VIAL, GLASS	PELLET	151		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10191-1585	SULPHUR (SULFUR) PELLET [REMEDY MAKERS]	2	Legacy NDC, 1 package rows	20100312_f0cbf8e3-6601-4955-a738-d6045a28835d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
SULFUR	ACTIVE INGREDIENT	70FD1KFU70	2
SULFUR	ACTIVE MOIETY	70FD1KFU70	2

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

SULPHUR
SULFUR

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10191-1585	10191-1585-2

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
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
21ccc2d5-c363-443e-9b43-2c5e1ae04e28			f0cbf8e3-6601-4955-a738-d6045a28835d	2010-03-12		Exact identifier spl id: 21ccc2d5-c363-443e-9b43-2c5e1ae04e28 spl set id: f0cbf8e3-6601-4955-a738-d6045a28835d

Reported adverse events (FAERS/openFDA)#

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