Home NDC 71714-004 Acne Gel Pen
Product NDC 71714-004
11-digit product format 717140004
Labeler code 71714
Product ID 71714-004_5d305187-3783-b840-e063-6394a90a1593
Type HUMAN OTC DRUG
Nonproprietary name Salicylic Acid
Dosage form GEL
Route TOPICAL
Labeler Tiege Hanley
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-10-31
Substance SALICYLIC ACID
Active strength 20 mg/mL
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 Acne Gel Pen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 20 mg/mL
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71714-004-01 Acne Gel Pen 1.3 mL in 1 TUBE, WITH APPLICATOR GEL 1.3 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 7 of 55 · 1,088 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 71714-004-01 71714000401 1.3 mL in 1 TUBE, WITH APPLICATOR (71714-004-01) 1.3 ml 2025-10-31 No No Current