Home NDC 76184-0101 DERMASIL DRYSKIN
Product NDC 76184-0101
11-digit product format 761840101
Labeler code 76184
Product ID 76184-0101_d08d5bc8-6935-4ff4-a223-c02c0887a904
Type HUMAN OTC DRUG
Nonproprietary name DIMETHICONE
Dosage form LOTION
Route TOPICAL
Labeler Fantasia Beauty LLC
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-08-30
Substance DIMETHICONE
Active strength .01 g/mL
Pharmacologic classes Skin Barrier Activity [PE]
NDC exclude flag No
Listing certified through 2026-12-31
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 DERMASIL DRYSKIN
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIMETHICONE .01 g/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 92RU3N3Y1O Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 199680 Internal RxNorm lookup 880878 Internal RxNorm 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 76184-0101-2 DERMASIL DRYSKIN 236 mL in 1 TUBE LOTION 236 4 76184-0101-3 DERMASIL DRYSKIN 429 mL in 1 BOTTLE LOTION 429 4 76184-0101-4 DERMASIL DRYSKIN 535 mL in 1 BOTTLE LOTION 535 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76184-0101 DERMASIL DRYSKIN (DIMETHICONE) LOTION [FANTASIA BEAUTY LLC] 4 Current NDC, Legacy NDC, 3 package rows 20250221_8a49f4be-8a73-41ca-86f4-11a707b2987a.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 59 of 68 · 1,357 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 76184-0101-1 76184010101 214 mL in 1 TUBE (76184-0101-1) 214 ml 2017-08-30 0000-00-00 No No Current 76184-0101-2 76184010102 236 mL in 1 TUBE (76184-0101-2) 236 ml 2017-08-30 0000-00-00 No No Current 76184-0101-3 76184010103 429 mL in 1 BOTTLE (76184-0101-3) 429 ml 2023-01-01 0000-00-00 No No Current 76184-0101-4 76184010104 535 mL in 1 BOTTLE (76184-0101-4) 535 ml 2023-11-01 0000-00-00 No No Current 76184-0101-5 76184010105 296 mL in 1 TUBE (76184-0101-5) 296 ml 2017-08-30 0000-00-00 No No Current 76184-0101-6 76184010106 296 mL in 1 BOTTLE (76184-0101-6) 296 ml 2017-08-30 0000-00-00 No No Current 76184-0101-7 76184010107 429 mL in 1 BOTTLE (76184-0101-7) 429 ml 2017-08-30 0000-00-00 No No Current 76184-0101-8 76184010108 535 mL in 1 BOTTLE (76184-0101-8) 535 ml 2017-08-30 0000-00-00 No No Current