LAMISIL AF

Product NDC
0067-6114
11-digit product format
000676114
Labeler code
0067
Product ID
0067-6114_27b9c3f2-4717-497f-994d-21096e3f3e15
Type
HUMAN OTC DRUG
Nonproprietary name
Tolnaftate
Dosage form
AEROSOL, SPRAY
Route
TOPICAL
Labeler
GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Application
part333C
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2006-02-01
Marketing end
2020-03-31
Substance
TOLNAFTATE
Active strength
10 mg/g
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0067-6114-46GM - Gram0067-611494c04464-93d9-4d27-8377-1164773cb0e512014-04-03