Home NDC 53645-1213 Hepar Sulf 30X
Product NDC 53645-1213
11-digit product format 536451213
Labeler code 53645
Product ID 53645-1213_4c1fee2b-f4f4-74c0-e063-6294a90a3094
Type HUMAN OTC DRUG
Nonproprietary name Hepar Sulf 30X
Dosage form LIQUID
Route ORAL
Labeler True Botanica, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-03-02
Substance CALCIUM SULFIDE
Active strength 30 [hp_X]/30mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Hepar Sulf 30X
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM SULFIDE 30 [hp_X]/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1MBW07J51Q Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 53645-1213-6 Hepar Sulf 30X 30 mL in 1 BOTTLE LIQUID 30 1
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 53645-1213-6 53645121306 30 mL in 1 BOTTLE (53645-1213-6) 30 ml 2026-03-02 No No Current