Aftertest Pain Relief

Product NDC
71814-410
11-digit product format
718140410
Labeler code
71814
Product ID
71814-410_cff907f1-e5bd-80bc-e053-2a95a90ae38a
Type
HUMAN OTC DRUG
Nonproprietary name
Benzocaine
Dosage form
STICK
Route
TOPICAL
Labeler
Diabetic Supply of Suncoast, Inc.
Application
part348
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2017-01-28
Marketing end
0000-00-00
Substance
BENZOCAINE
Active strength
100 mg/mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71814-410-012021-11-04C16284748780-19d75b9d0-e428-f424-e053-dadaa90a57ce1469366a-5e93-4a2c-96b6-425b1cc7b2d9
71814-410-012020-01-31C16284748780-19d75b9d0-e428-f424-e053-dadaa90a57ce1469366a-5e93-4a2c-96b6-425b1cc7b2d9

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71814-410-01ML - Milliliter71814-410b7728e13-e98a-4972-99d0-a4f434f6dce712017-12-14