UP AND UP NO DRIP NASAL

Product NDC
82442-388
11-digit product format
824420388
Labeler code
82442
Product ID
82442-388_b4146c3c-25f4-441c-a99b-bbbeb817a105
Type
HUMAN OTC DRUG
Nonproprietary name
Oxymetazoline Hydrochloride
Dosage form
SPRAY
Route
NASAL
Labeler
Target Corporation
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-01-24
Substance
OXYMETAZOLINE HYDROCHLORIDE
Active strength
.05 g/100mL
Pharmacologic classes
Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
K89MJ0S5VYOXYMETAZOLINE HYDROCHLORIDE2315-02-8OXYMETAZOLINE HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
82442-388-10824420388101 BOTTLE, SPRAY in 1 CARTON (82442-388-10) / 30 mL in 1 BOTTLE, SPRAY2025-01-24NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Target Corporation No Drip Nasal Spray Drug FactsTarget Corporation2025-01-29HUMAN OTC DRUG LABEL2