up and up nasal
Generic: oxymetazoline hydrochloride
Labeler: target corporationDrug Facts
Product Profile
Brand Name
up and up nasal
Generic Name
oxymetazoline hydrochloride
Labeler
target corporation
Dosage Form
SPRAY
Routes
Active Ingredients
oxymetazoline hydrochloride .05 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
11673-304
Product ID
11673-304_9211198c-c1b8-493d-b7ee-3a9073815388
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2009-08-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
11673304
Hyphenated Format
11673-304
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
up and up nasal (source: ndc)
Generic Name
oxymetazoline hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .05 g/100mL
Packaging
- 1 BOTTLE, SPRAY in 1 CARTON (11673-304-10) / 30 mL in 1 BOTTLE, SPRAY
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "9211198c-c1b8-493d-b7ee-3a9073815388", "openfda": {"unii": ["K89MJ0S5VY"], "rxcui": ["1000990"], "spl_set_id": ["0c246c11-eadd-4ac6-bd58-5fdb151e06d6"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 CARTON (11673-304-10) / 30 mL in 1 BOTTLE, SPRAY", "package_ndc": "11673-304-10", "marketing_start_date": "20090812"}], "brand_name": "Up and up nasal", "product_id": "11673-304_9211198c-c1b8-493d-b7ee-3a9073815388", "dosage_form": "SPRAY", "pharm_class": ["Imidazolines [CS]", "Increased Sympathetic Activity [PE]", "Vasoconstriction [PE]", "Vasoconstrictor [EPC]"], "product_ndc": "11673-304", "generic_name": "oxymetazoline hydrochloride", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Up and up nasal", "active_ingredients": [{"name": "OXYMETAZOLINE HYDROCHLORIDE", "strength": ".05 g/100mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20090812", "listing_expiration_date": "20261231"}