Package 11673-186-40
Brand: up and up nighttime sleep aid
Generic: diphenhydramine hydrochloridePackage Facts
Identity
Package NDC
11673-186-40
Digits Only
1167318640
Product NDC
11673-186
Description
355 mL in 1 BOTTLE (11673-186-40)
Marketing
Marketing Status
Brand
up and up nighttime sleep aid
Generic
diphenhydramine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8a241401-903d-483a-b45e-68347db69c72", "openfda": {"unii": ["TC2D6JAD40"], "spl_set_id": ["0ab5a374-d565-4385-bee3-538a8f09b19e"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (11673-186-40)", "package_ndc": "11673-186-40", "marketing_start_date": "20200326"}], "brand_name": "Up and Up Nighttime Sleep Aid", "product_id": "11673-186_8a241401-903d-483a-b45e-68347db69c72", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "11673-186", "generic_name": "diphenhydramine hydrochloride", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Up and Up Nighttime Sleep Aid", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/30mL"}], "application_number": "M010", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200326", "listing_expiration_date": "20261231"}