Sulfur 30X

Product NDC
53645-1203
11-digit product format
536451203
Labeler code
53645
Product ID
53645-1203_254f573d-6268-8338-e063-6394a90a408c
Type
HUMAN OTC DRUG
Nonproprietary name
SULFUR
Dosage form
LIQUID
Route
ORAL
Labeler
True Botanica, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2025-04-01
Substance
SULFUR
Active strength
30 [hp_X]/30mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Sulfur 30X
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SULFUR30 [hp_X]/30mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53645-1203-6Sulfur 30X30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53645-1203SULFUR 30X (SULFUR) LIQUID [TRUE BOTANICA, LLC]1Current NDC, 1 package rows20250403_254f4c7d-0569-53b0-e063-6294a90a59f2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
53645-1203-65364512030630 mL in 1 BOTTLE (53645-1203-6) 30 ml2025-04-01NoNoHistorical