Home NDC 84867-030-01 BUNUSS Phyto-Pro Skin Cream
Product NDC 84867-030
Requested package NDC 84867-030-01
11-digit product format 848670030
Labeler code 84867
Product ID 84867-030_44e1ec89-e2eb-d438-e063-6294a90a41f4
Type HUMAN OTC DRUG
Nonproprietary name PROGESTERONE
Dosage form PASTE
Route TOPICAL
Labeler Jiashen International Trade Limited
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2025-12-01
Substance PROGESTERONE
Active strength 16.9 mg/mL
Pharmacologic classes Progesterone [CS], Progesterone [EPC]
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 BUNUSS Phyto-Pro Skin Cream
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PROGESTERONE 16.9 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4G7DS2Q64Y 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 84867-030-01 BUNUSS Phyto-Pro Skin Cream 120 mL in 1 BOTTLE PASTE 120 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 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 84867-030-01 84867003001 120 mL in 1 BOTTLE (84867-030-01) 120 ml 2025-12-01 No No Current