Package 21130-807-10
Brand: nasal decongestant
Generic: oxymetazoline hydrochloridePackage Facts
Identity
Package NDC
21130-807-10
Digits Only
2113080710
Product NDC
21130-807
Description
1 BOTTLE, SPRAY in 1 CARTON (21130-807-10) / 30 mL in 1 BOTTLE, SPRAY
Marketing
Marketing Status
Brand
nasal decongestant
Generic
oxymetazoline hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "43db7f87-29db-4c9d-9257-bb6e5c402443", "openfda": {"unii": ["K89MJ0S5VY"], "rxcui": ["1000990"], "spl_set_id": ["f1d0edd5-fe58-4de0-98f4-07fb24bd0ac2"], "manufacturer_name": ["Safeway"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 CARTON (21130-807-10) / 30 mL in 1 BOTTLE, SPRAY", "package_ndc": "21130-807-10", "marketing_start_date": "20250214"}], "brand_name": "nasal decongestant", "product_id": "21130-807_43db7f87-29db-4c9d-9257-bb6e5c402443", "dosage_form": "SPRAY", "pharm_class": ["Imidazolines [CS]", "Increased Sympathetic Activity [PE]", "Vasoconstriction [PE]", "Vasoconstrictor [EPC]"], "product_ndc": "21130-807", "generic_name": "Oxymetazoline Hydrochloride", "labeler_name": "Safeway", "product_type": "HUMAN OTC DRUG", "brand_name_base": "nasal decongestant", "active_ingredients": [{"name": "OXYMETAZOLINE HYDROCHLORIDE", "strength": ".05 g/100mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250214", "listing_expiration_date": "20261231"}