FDA.reportPublic FDA data

Sulphur

Manufacturer
Newton Laboratories, Inc.
Effective date
2023-04-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:20:53

Label at a glance#

ProductSulphur
Active ingredientSULFUR
Label structure10 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Unhealthy hair and skin; Burning with itching; Burning in eyes; Diarrhea; Dizziness

DOSAGE & ADMINISTRATION SECTION

Directions: Ages 12 and up, take 6 drops by mouth, (ages 0 to 11, give 3 drops) as needed or as directed by a health professional.

OTC - ACTIVE INGREDIENT SECTION

Sulphur 9x

OTC - PURPOSE SECTION

Unhealthy hair and skin; Burning with itching; Burning in eyes; Diarrhea; Dizziness

INACTIVE INGREDIENT SECTION

Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane alcohol 20%.

QUESTIONS SECTION

OTC - QUESTIONS SECTION

newtonlabs.net – Questions? 800.448.7256

Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013

WARNINGS SECTION

Warning:Keep out of reach of children. Do not use if tamper - evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55714-9023-6Sulphur3 L in 1 BOTTLE, PLASTICLIQUID31

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55714-9023SULPHUR LIQUID [NEWTON LABORATORIES, INC.]1Current NDC, 1 package rows20230412_f9142532-84eb-1e4f-e053-6394a90afc15.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
55714-902355714-9023-6

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
SULFUR70FD1KFU70ACTIB

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
SulphurSULPHURNewton Laboratories, Inc.f9142532-84eb-1e4f-e053-6394a90afc152023-04-11WarningsExact identifier
ndc (package): 55714-9023-6
ndc (product): 55714-9023
ndc11 (package): 55714902306
spl id: f913ff17-b570-003e-e053-6294a90a5536
spl set id: f9142532-84eb-1e4f-e053-6394a90afc15

Reported adverse events (FAERS/openFDA)#

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