Home NDC 69683-202 DERMOSCRIBE SEBORRHEIC DERMATITIS
Product NDC 69683-202
11-digit product format 696830202
Labeler code 69683
Product ID 69683-202_4161aee0-5f36-1739-e063-6294a90a5bdf
Type HUMAN OTC DRUG
Nonproprietary name SULFUR, SALICYLIC ACID, HYDROCORTISONE
Dosage form CREAM
Route TOPICAL
Labeler DERMOSCRIBE PTY LTD
Application M032
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-03-23
Substance SULFUR; SALICYLIC ACID; HYDROCORTISONE
Active strength 3; 3; 1 g/100g; g/100g; g/100g
Pharmacologic classes Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
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 DERMOSCRIBE SEBORRHEIC DERMATITIS
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFUR 3 g/100g SALICYLIC ACID 3 g/100g HYDROCORTISONE 1 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 70FD1KFU70 Internal UNII lookup O414PZ4LPZ Internal UNII lookup WI4X0X7BPJ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1738574 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69683-202-11 DERMOSCRIBE SEBORRHEIC DERMATITIS 60 g in 1 BOTTLE CREAM 60 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69683-202 DERMOSCRIBE SEBORRHEIC DERMATITIS (SULFUR, SALICYLIC ACID, HYDROCORTISONE) CREAM [DERMOSCRIBE PTY LTD] 8 Current NDC, Legacy NDC, 1 package rows 20241109_2b6bf90b-5d42-4c08-afee-56e13122285e.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 16 of 31 · 615 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 69683-202-11 69683020211 60 g in 1 BOTTLE (69683-202-11) 60 g 2015-03-23 0000-00-00 No No Current