Home NDC 60717-412 Texture ID Anti Dandruff Oil Treatment
Product NDC 60717-412
11-digit product format 607170412
Labeler code 60717
Product ID 60717-412_450ec8ae-2406-8d2f-e063-6394a90a50db
Type HUMAN OTC DRUG
Nonproprietary name Salicylic Acid
Dosage form OIL
Route TOPICAL
Labeler RNA PHARMA, LLC
Application M014
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-09-25
Substance SALICYLIC ACID
Active strength .02 g/g
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 Texture ID Anti Dandruff Oil Treatment
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID .02 g/g
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 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 60717-412-04 Texture ID Anti Dandruff Oil Treatment 1 g in 1 BOTTLE OIL 1 1
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 4 of 7 · 135 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 60717-412-04 60717041204 1 g in 1 BOTTLE (60717-412-04) 1 g 2025-09-25 No No Current