Leader Oral Pain Relief

Product NDC
37205-607
11-digit product format
372050607
Labeler code
37205
Product ID
37205-607_de03e285-4967-460e-8843-0b874dd1d203
Type
HUMAN OTC DRUG
Nonproprietary name
Benzocaine 20%
Dosage form
GEL
Route
ORAL
Labeler
Cardinal Health
Application
part356
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2012-08-08
Marketing end
0000-00-00
Substance
BENZOCAINE
Active strength
200 mg/g
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
37205-607-062025-04-28C16284748780-19d75b9d1-087f-f424-e053-dadaa90a57ce72274fff-065b-4c87-9207-68ee8a537618
37205-607-062020-01-31C16284748780-19d75b9d1-087f-f424-e053-dadaa90a57ce72274fff-065b-4c87-9207-68ee8a537618