n-Drops NASAL DECONGESTANT

Product NDC
73921-010
11-digit product format
739210010
Labeler code
73921
Product ID
73921-010_96e30859-36c5-4aa7-9b3d-9262c773c971
Type
HUMAN OTC DRUG
Nonproprietary name
Oxymetazoline Hydrochloride
Dosage form
SPRAY
Route
NASAL
Labeler
GLOBAL PHARMA HEALTHCARE PRIVATE LIMITED
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-04-01
Marketing end
0000-00-00
Substance
OXYMETAZOLINE HYDROCHLORIDE
Active strength
1 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
73921-010-152023-02-08C16284748780-1f386c649-cdef-0266-e053-dadaa90a7c1af96dc26e-67bd-4c70-bb8a-5b66b96b2af5
73921-010-152023-01-30C16284748780-1f386c649-cdef-0266-e053-dadaa90a7c1af96dc26e-67bd-4c70-bb8a-5b66b96b2af5

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
73921-010-15739210010151 BOTTLE, SPRAY in 1 CARTON (73921-010-15) > 15 mL in 1 BOTTLE, SPRAY2021-04-010000-00-00NoNoCurrent