Home NDC 76354-210 ELF Blemish Control Face Primer Clear
Product NDC 76354-210
11-digit product format 763540210
Labeler code 76354
Product ID 76354-210_2641d44b-d93a-d724-e063-6394a90a58fb
Type HUMAN OTC DRUG
Nonproprietary name SALICYLIC ACID
Dosage form CREAM
Route TOPICAL
Labeler e.l.f. Cosmetics, Inc
Application M032
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-08-17
Substance SALICYLIC ACID
Active strength 2 g/100mL
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 ELF Blemish Control Face Primer Clear
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 2 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O414PZ4LPZ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 317152 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 76354-210-10 ELF Blemish Control Face Primer Clear 30 mL in 1 BOTTLE CREAM 30 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76354-210 ELF BLEMISH CONTROL FACE PRIMER CLEAR (SALICYLIC ACID) CREAM [E.L.F. COSMETICS, INC] 8 Current NDC, Legacy NDC, 1 package rows 20241108_21bdbc81-d243-439b-ac90-31d9107222b4.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 31 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 76354-210-10 76354021010 30 mL in 1 BOTTLE (76354-210-10) 30 ml 2017-08-17 0000-00-00 No No Current