Home NDC 85053-005 WOODSLEEP Wild Yam Cream
Product NDC 85053-005
11-digit product format 850530005
Labeler code 85053
Product ID 85053-005_53b992fd-575a-57bb-e063-6394a90a1600
Type HUMAN OTC DRUG
Nonproprietary name GLYCERIN
Dosage form CREAM
Route TOPICAL
Labeler Shantou Woodsleep Biotechnology Co., Ltd.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-08
Substance DIOSCOREA VILLOSA ROOT
Active strength .02 mg/100mg
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 WOODSLEEP Wild Yam Cream
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIOSCOREA VILLOSA ROOT .02 mg/100mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination IWY3IWX2G8 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 44 of 68 · 1,357 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85053-005-01 85053000501 100 mg in 1 BOTTLE, PLASTIC (85053-005-01) 100 mg 2026-06-08 No No Current