Oxalis 20%

Product NDC
48951-7198
11-digit product format
489517198
Labeler code
48951
Product ID
48951-7198_cf32aa91-9c59-1e02-e053-2a95a90ab611
Type
HUMAN OTC DRUG
Nonproprietary name
Oxalis 20%
Dosage form
CREAM
Route
TOPICAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
OXALIS STRICTA WHOLE
Active strength
1 [hp_X]/g
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-7198-5Oxalis 20%60 g in 1 TUBECREAM602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-7198OXALIS 20% CREAM [URIEL PHARMACY INC.]2Legacy NDC, 1 package rows20240514_cf32aa91-9c58-1e02-e053-2a95a90ab611.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-7198-54895171980560 g in 1 TUBE (48951-7198-5) 60 g2009-09-010000-00-00NoNoCurrent