Package 11673-771-01
Brand: up and up dry eye relief lubricant eye drops
Generic: carboxymethylcellulose sodiumPackage Facts
Identity
Package NDC
11673-771-01
Digits Only
1167377101
Product NDC
11673-771
Description
2 BOTTLE, DROPPER in 1 BOX (11673-771-01) / 15 mL in 1 BOTTLE, DROPPER
Marketing
Marketing Status
Brand
up and up dry eye relief lubricant eye drops
Generic
carboxymethylcellulose sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "4202718c-a8c4-9344-e063-6394a90ace0f", "openfda": {"upc": ["0095072089008"], "unii": ["K679OBS311"], "rxcui": ["1188426"], "spl_set_id": ["3b1834e6-75cf-5380-e063-6294a90ad1d5"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BOTTLE, DROPPER in 1 BOX (11673-771-01) / 15 mL in 1 BOTTLE, DROPPER", "package_ndc": "11673-771-01", "marketing_start_date": "20251031"}], "brand_name": "Up and Up Dry Eye Relief Lubricant Eye Drops", "product_id": "11673-771_4202718c-a8c4-9344-e063-6394a90ace0f", "dosage_form": "SOLUTION/ DROPS", "product_ndc": "11673-771", "generic_name": "Carboxymethylcellulose Sodium", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Up and Up Dry Eye Relief Lubricant Eye Drops", "active_ingredients": [{"name": "CARBOXYMETHYLCELLULOSE SODIUM", "strength": "5 mg/mL"}], "application_number": "M018", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251031", "listing_expiration_date": "20261231"}