Home NDC 87019-001 Escozul
Product NDC 87019-001
11-digit product format 870190001
Labeler code 87019
Product ID 87019-001_acee59b0-ff10-452a-a3ce-805008614908
Type HUMAN OTC DRUG
Nonproprietary name RHOPALURUS JUNCEUS VENOM
Dosage form SOLUTION/ DROPS
Route ORAL
Labeler Blue Scorpion Group INC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-10-01
Substance RHOPALURUS JUNCEUS VENOM
Active strength 6 [hp_X]/mL
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 Escozul
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength RHOPALURUS JUNCEUS VENOM 6 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination K1XKC8OD5S Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87019-001-01 Escozul 60 mL in 1 BOTTLE SOLUTION/ DROPS 60 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 87019-001-01 87019000101 60 mL in 1 BOTTLE (87019-001-01) 60 ml 2025-10-01 No No Current