Home NDC 43479-106 EradiKate ACNE TREATMENT
Product NDC 43479-106
11-digit product format 434790106
Labeler code 43479
Product ID 43479-106_2b826d62-b44e-974d-e063-6394a90a109d
Type HUMAN OTC DRUG
Nonproprietary name SULFUR
Dosage form LIQUID
Route TOPICAL
Labeler Kate Somerville Skincare, LLC
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-06-15
Substance SULFUR
Active strength 10 g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 14 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 43479-106-51 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 43479-106-51 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 43479-106-51 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 43479-106-51 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 43479-106-51 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 43479-106-51 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 43479-106-51 1332a3947898…d4bfe170f9cd…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base EradiKate ACNE TREATMENT
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFUR 10 g/100mL
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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198869 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43479-106-11 EradiKate ACNE TREATMENT 30 mL in 1 BOTTLE, GLASS LIQUID 30 8 43479-106-51 EradiKate ACNE TREATMENT 1 in 1 BOX LIQUID 1 8
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SULFUR ACTIVE INGREDIENT 70FD1KFU70 ERADIKATE ACNE TREATMENT (SULFUR) LIQUID [KATE SOMERVILLE SKINCARE, LLC] 1 SULFUR ACTIVE MOIETY 70FD1KFU70 ERADIKATE ACNE TREATMENT (SULFUR) LIQUID [KATE SOMERVILLE SKINCARE, LLC] 1 CAMPHOR (NATURAL) INACTIVE INGREDIENT N20HL7Q941 ERADIKATE ACNE TREATMENT (SULFUR) LIQUID [KATE SOMERVILLE SKINCARE, LLC] 1 FERRIC OXIDE RED INACTIVE INGREDIENT 1K09F3G675 ERADIKATE ACNE TREATMENT (SULFUR) LIQUID [KATE SOMERVILLE SKINCARE, LLC] 1 FERRIC OXIDE YELLOW INACTIVE INGREDIENT EX438O2MRT ERADIKATE ACNE TREATMENT (SULFUR) LIQUID [KATE SOMERVILLE SKINCARE, LLC] 1 FERROSOFERRIC OXIDE INACTIVE INGREDIENT XM0M87F357 ERADIKATE ACNE TREATMENT (SULFUR) LIQUID [KATE SOMERVILLE SKINCARE, LLC] 1 FERROUS OXIDE INACTIVE INGREDIENT G7036X8B5H ERADIKATE ACNE TREATMENT (SULFUR) LIQUID [KATE SOMERVILLE SKINCARE, LLC] 1 ISOPROPYL ALCOHOL INACTIVE INGREDIENT ND2M416302 ERADIKATE ACNE TREATMENT (SULFUR) LIQUID [KATE SOMERVILLE SKINCARE, LLC] 1 MAGNESIUM ALUMINUM SILICATE INACTIVE INGREDIENT 6M3P64V0NC ERADIKATE ACNE TREATMENT (SULFUR) LIQUID [KATE SOMERVILLE SKINCARE, LLC] 1 SALICYLIC ACID INACTIVE INGREDIENT O414PZ4LPZ ERADIKATE ACNE TREATMENT (SULFUR) LIQUID [KATE SOMERVILLE SKINCARE, LLC] 1 WATER INACTIVE INGREDIENT 059QF0KO0R ERADIKATE ACNE TREATMENT (SULFUR) LIQUID [KATE SOMERVILLE SKINCARE, LLC] 1 ZINC OXIDE INACTIVE INGREDIENT SOI2LOH54Z ERADIKATE ACNE TREATMENT (SULFUR) LIQUID [KATE SOMERVILLE SKINCARE, LLC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43479-106 ERADIKATE ACNE TREATMENT (SULFUR) LIQUID [KATE SOMERVILLE SKINCARE, LLC] 8 Current NDC, Legacy NDC, 2 package rows 20250113_713093d9-29c3-44c9-b90f-ee7448c5063e.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 48 of 54 · 1,079 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43479-106-11 43479010611 30 mL in 1 BOTTLE, GLASS 30 ml Historical 43479-106-51 43479010651 1 BOTTLE, GLASS in 1 BOX (43479-106-51) / 30 mL in 1 BOTTLE, GLASS (43479-106-11) 2014-06-15 0000-00-00 No No Current