Home NDC 43406-0472 Sulphur 30C
Product NDC 43406-0472
11-digit product format 434060472
Labeler code 43406
Product ID 43406-0472_79e6debb-b348-4f5c-a177-ed059ba0406d
Type HUMAN OTC DRUG
Nonproprietary name Sulphur
Dosage form LIQUID
Route ORAL
Labeler Natural Creations, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2012-06-18
Substance SULFUR
Active strength 30 [hp_C]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Sulphur 30C
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFUR 30 [hp_C]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 70FD1KFU70 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 43406-0472-1 Sulphur 30C 30 mL in 1 BOTTLE, DROPPER LIQUID 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43406-0472 SULPHUR 30C (SULPHUR) LIQUID [NATURAL CREATIONS, INC] 1 Current NDC, Legacy NDC, 1 package rows 20230111_32c0d686-0732-47b6-9c05-943651d2814f.zip
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 Marketing end Sample Exclude flag Status 43406-0472-1 43406047201 30 mL in 1 BOTTLE, DROPPER (43406-0472-1) 30 ml 2012-06-18 0000-00-00 No No Current