Package 37808-956-12
Brand: h.e.b solutions sunscreen
Generic: ultra spf 50 lotionPackage Facts
Identity
Package NDC
37808-956-12
Digits Only
3780895612
Product NDC
37808-956
Description
237 mL in 1 TUBE (37808-956-12)
Marketing
Marketing Status
Brand
h.e.b solutions sunscreen
Generic
ultra spf 50 lotion
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "248a0777-7394-dea1-e063-6394a90a444a", "openfda": {"upc": ["0041220898954", "0041220898930"], "unii": ["G63QQF2NOX", "V06SV4M95S", "4X49Y0596W", "5A68WGF6WM", "95OOS7VE0Y"], "spl_set_id": ["12c76c72-4411-48d5-b79b-c58703bf1fdd"], "manufacturer_name": ["H.E.B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "89 mL in 1 TUBE (37808-956-09)", "package_ndc": "37808-956-09", "marketing_start_date": "20120220"}, {"sample": false, "description": "237 mL in 1 TUBE (37808-956-12)", "package_ndc": "37808-956-12", "marketing_start_date": "20120220"}], "brand_name": "H.E.B Solutions Sunscreen", "product_id": "37808-956_248a0777-7394-dea1-e063-6394a90a444a", "dosage_form": "LOTION", "product_ndc": "37808-956", "generic_name": "Ultra SPF 50 Lotion", "labeler_name": "H.E.B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "H.E.B", "brand_name_suffix": "Solutions Sunscreen", "active_ingredients": [{"name": "AVOBENZONE", "strength": "20 mg/mL"}, {"name": "HOMOSALATE", "strength": "100 mg/mL"}, {"name": "OCTISALATE", "strength": "50 mg/mL"}, {"name": "OCTOCRYLENE", "strength": "70 mg/mL"}, {"name": "OXYBENZONE", "strength": "60 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120220", "listing_expiration_date": "20261231"}