Home NDC 11086-028 LIQUIMAT
Product NDC 11086-028
11-digit product format 110860028
Labeler code 11086
Product ID 11086-028_5d2dc370-2253-98c4-e063-6394a90a8224
Type HUMAN OTC DRUG
Nonproprietary name SULFUR
Dosage form LIQUID
Route TOPICAL
Labeler Summers Laboratories Inc
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-10-30
Substance SULFUR
Active strength 3 g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 LIQUIMAT
Brand name suffix ACNE TREATMENT AND COVER-UP
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFUR 3 g/100mL
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11086-028-01 LIQUIMATACNE TREATMENT AND COVER-UP 44 mL in 1 BOTTLE LIQUID 44 11
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11086-028 LIQUIMAT ACNE TREATMENT AND COVER-UP (SULFUR) LIQUID [SUMMERS LABORATORIES INC] 10 Current NDC, Legacy NDC, 1 package rows 20240405_3cb843ad-f52a-4876-b844-d441af08b27f.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 33 of 55 · 1,088 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 11086-028-01 11086002801 44 mL in 1 BOTTLE (11086-028-01) 44 ml 2013-10-30 0000-00-00 No No Current