Home NDC 48951-7214 Oxalis 1X
Product NDC 48951-7214
11-digit product format 489517214
Labeler code 48951
Product ID 48951-7214_2c907346-28ec-f243-e063-6294a90ae572
Type HUMAN OTC DRUG
Nonproprietary name Oxalis 1X
Dosage form OINTMENT
Route TOPICAL
Labeler Uriel Pharmacy, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance OXALIS STRICTA WHOLE
Active strength 1 [hp_X]/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Oxalis 1X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OXALIS STRICTA WHOLE 1 [hp_X]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3STW243384 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 48951-7214-2 Oxalis 1X 30 g in 1 TUBE OINTMENT 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-7214 OXALIS 1X OINTMENT [URIEL PHARMACY, INC] 1 Current NDC, 1 package rows 20250127_2c907346-28eb-f243-e063-6294a90ae572.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 Sample Exclude flag Status 48951-7214-2 48951721402 30 g in 1 TUBE (48951-7214-2) 30 g 2009-09-01 No No Current