Package 69790-849-08
Brand: alcohol
Generic: alcoholPackage Facts
Identity
Package NDC
69790-849-08
Digits Only
6979084908
Product NDC
69790-849
Description
3785 mL in 1 BOTTLE, PLASTIC (69790-849-08)
Marketing
Marketing Status
Brand
alcohol
Generic
alcohol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4b09a991-ce1b-ead1-e063-6294a90afce2", "openfda": {"unii": ["3K9958V90M"], "spl_set_id": ["fdda41fa-d847-4cee-a070-91f0600b0fc8"], "manufacturer_name": ["Uline"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3785 mL in 1 BOTTLE, PLASTIC (69790-849-08)", "package_ndc": "69790-849-08", "marketing_start_date": "20190719"}, {"sample": false, "description": "2082 mL in 1 DRUM (69790-849-55)", "package_ndc": "69790-849-55", "marketing_start_date": "20200814"}], "brand_name": "Alcohol", "product_id": "69790-849_4b09a991-ce1b-ead1-e063-6294a90afce2", "dosage_form": "LIQUID", "product_ndc": "69790-849", "generic_name": "Alcohol", "labeler_name": "Uline", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alcohol", "active_ingredients": [{"name": "ALCOHOL", "strength": "62 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190719", "listing_expiration_date": "20271231"}