Home NDC 87714-002 MOUTH ULCER
Product NDC 87714-002
11-digit product format 877140002
Labeler code 87714
Product ID 87714-002_5264f81c-bfff-4f6d-e063-6394a90ae3bf
Type HUMAN OTC DRUG
Nonproprietary name panthenol
Dosage form LIQUID
Route BUCCAL
Labeler Guangzhou Shengli Shidai Cosmetics Co., Ltd.
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-05-22
Substance PANTHENOL
Active strength 1.2 g/100mL
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 MOUTH ULCER
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PANTHENOL 1.2 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination WV9CM0O67Z 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 87714-002-01 MOUTH ULCER 20 mL in 1 BOTTLE LIQUID 20 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 29 of 40 · 786 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87714-002-01 87714000201 20 mL in 1 BOTTLE (87714-002-01) 20 ml 2026-05-22 No No Current