Home NDC 87947-001 Pharmlitalia Vaginal Symptoms Relief
Product NDC 87947-001
11-digit product format 879470001
Labeler code 87947
Product ID 87947-001_5a718a58-4abe-6bfc-e063-6394a90ac4bd
Type HUMAN OTC DRUG
Nonproprietary name Borax,Calendula officinalis,Hydrastis canadensis,Olive Extract
Dosage form GEL
Route VAGINAL
Labeler Guangzhou Trading Financing Union LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-08-18
Substance SODIUM BORATE; CALENDULA OFFICINALIS WHOLE; GOLDENSEAL; OLEUROPEIN
Active strength 3; 1; 5; 3 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/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 Pharmlitalia Vaginal Symptoms Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM BORATE 3 [hp_X]/g CALENDULA OFFICINALIS WHOLE 1 [hp_X]/g GOLDENSEAL 5 [hp_X]/g OLEUROPEIN 3 [hp_X]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 87947-001-01 87947000101 12.1 g in 1 APPLICATOR (87947-001-01) 12.1 g 2026-08-18 No No Current