Nasal Decongestant PE

Product NDC
37835-651
11-digit product format
378350651
Labeler code
37835
Product ID
37835-651_3127723a-459d-0ab2-e063-6394a90ad329
Type
HUMAN OTC DRUG
Nonproprietary name
PHENYLEPHRINE HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
Bi-Mart
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-03-01
Substance
PHENYLEPHRINE HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Nasal Decongestant PE
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PHENYLEPHRINE HYDROCHLORIDE10 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii04JA59TNSJ
Rxcui1049182

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37835-651-01Nasal Decongestant PE100 in 1 BOTTLETABLET1001
37835-651-36Nasal Decongestant PE36 in 1 BOTTLETABLET361

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37835-651NASAL DECONGESTANT PE (PHENYLEPHRINE HYDROCHLORIDE) TABLET [BI-MART]1Current NDC, 2 package rows20250327_d208cb6f-e142-4aa3-959b-e6b601df76c1.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049182phenylephrine HCl 10 MG Oral TabletPSNd208cb6f-e142-4aa3-959b-e6b601df76c11
1049182phenylephrine hydrochloride 10 MG Oral TabletSCDd208cb6f-e142-4aa3-959b-e6b601df76c11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37835-651-0137835065101100 TABLET in 1 BOTTLE (37835-651-01) 100 tablet2025-03-01NoNoCurrent
37835-651-363783506513636 TABLET in 1 BOTTLE (37835-651-36) 36 tablet2025-03-01NoNoCurrent