SUNMED Topical with Menthol

Product NDC
73240-903
11-digit product format
732400903
Labeler code
73240
Product ID
73240-903_db6f83c3-c17e-b253-e053-2995a90a5cc2
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
SPRAY
Route
TOPICAL
Labeler
Sunflora Inc.
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2022-03-30
Marketing end
0000-00-00
Substance
MENTHOL
Active strength
11 g/100g
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73240-903-012024-01-30C16284748780-11030e365-4f5a-111a-e063-dadaa90a10e2db6f7da5-aed6-cb18-e053-2995a90abbfc

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73240-903-017324009030189 g in 1 BOTTLE, SPRAY (73240-903-01) 89 g2022-03-300000-00-00NoNoCurrent