Home NDC 87541-737 Poison Ivy and Oak
Product NDC 87541-737
11-digit product format 875410737
Labeler code 87541
Product ID 87541-737_57245851-b9de-e8c4-e063-6294a90a9bea
Type HUMAN OTC DRUG
Nonproprietary name Poison Ivy and Oak
Dosage form SOAP
Route TOPICAL
Labeler Marie's Original Formulas LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-07-22
Substance SALIX ALBA BARK; SASSAFRAS ALBIDUM ROOT BARK; GRINDELIA CAMPORUM FLOWER/LEAF
Active strength 1; 1; 1 [hp_C]/g; [hp_C]/g; [hp_C]/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 Poison Ivy and Oak
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALIX ALBA BARK 1 [hp_C]/g SASSAFRAS ALBIDUM ROOT BARK 1 [hp_C]/g GRINDELIA CAMPORUM FLOWER/LEAF 1 [hp_C]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 205MXS71H7 Internal UNII lookup XC5UMP9I5F Internal UNII lookup IDB0NAZ6AI 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 87541-737-65 87541073765 82.2 g in 1 CARTON (87541-737-65) 82.2 g 2026-07-22 No No Current