FDA.reportPublic FDA data

Sulfur 3X

Product NDC
48951-8377
11-digit product format
489518377
Labeler code
48951
Product ID
48951-8377_c85c853f-d818-c72f-e053-2a95a90a18d5
Type
HUMAN OTC DRUG
Nonproprietary name
Sulfur 3X
Dosage form
POWDER
Route
TOPICAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-09
Marketing end
0000-00-00
Substance
SULFUR
Active strength
3 [hp_X]/g
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct48951-8377IInactivated by FDA2026-10-02
excluded packagepackage48951-837748951-8377-4IInactivated by FDA2026-10-02

Reported adverse events (FAERS/openFDA)#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8377-4Sulfur 3X50 g in 1 BOTTLE, GLASSPOWDER502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8377SULFUR 3X POWDER [URIEL PHARMACY INC.]2Legacy NDC, 1 package rows20210731_c702f426-b204-1fb3-e053-2995a90ad429.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8377-44895183770450 g in 1 BOTTLE, GLASS (48951-8377-4) 50 g2009-09-090000-00-00NoNoCurrent