Home NDC 37662-0740 Formica Rufa
Product NDC 37662-0740
11-digit product format 376620740
Labeler code 37662
Product ID 37662-0740_e32972ed-96e0-73f4-e053-2a95a90a61da
Type HUMAN OTC DRUG
Nonproprietary name Formica Rufa
Dosage form PELLET
Route ORAL
Labeler Hahnemann Laboratories, INC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-07-06
Substance FORMICA RUFA
Active strength 1 [hp_Q]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Formica Rufa
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FORMICA RUFA 1 [hp_Q]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 55H0W83JO5 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 37662-0740-1 Formica Rufa 10000 in 1 BOTTLE, GLASS PELLET 10000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37662-0740 FORMICA RUFA PELLET [HAHNEMANN LABORATORIES, INC.] 1 Current NDC, Legacy NDC, 1 package rows 20220708_e32972ed-96df-73f4-e053-2a95a90a61da.zip
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 Marketing end Sample Exclude flag Status 37662-0740-1 37662074001 10000 PELLET in 1 BOTTLE, GLASS (37662-0740-1) 10000 pellet 2022-07-06 0000-00-00 No No Current