Home NDC 87899-001 V-Fresh Restore Gel
Product NDC 87899-001
11-digit product format 878990001
Labeler code 87899
Product ID 87899-001_57b82e44-016a-8577-e063-6294a90ad1a9
Type HUMAN OTC DRUG
Nonproprietary name Sophora alopecuroides L
Dosage form GEL
Route TOPICAL
Labeler Shenzhen Xixi Beauty Industry Co., Ltd.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-29
Substance SOPHORA ALOPECUROIDES WHOLE
Active strength .2 g/g
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 V-Fresh Restore Gel
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SOPHORA ALOPECUROIDES WHOLE .2 g/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2MEL770SC5 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87899-001-01 87899000101 5 TUBE in 1 BOX (87899-001-01) / 3 g in 1 TUBE 5 tube 2026-07-29 No No Current