Package 37808-914-12

Brand: h.e.b ultra

Generic: spf 50 sunscreen
NDC Package

Package Facts

Identity

Package NDC 37808-914-12
Digits Only 3780891412
Product NDC 37808-914
Product ID 37808-914_c6b84cf6-4361-5352-e053-2995a90a2717
Description

237 mL in 1 TUBE (37808-914-12)

Marketing

Marketing Status
Marketed Since 2019-02-05
Brand h.e.b ultra
Generic spf 50 sunscreen
Sample Package No

Linked Drug Pages (1)

H.E.B ULTRA ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "c6b84cf6-4361-5352-e053-2995a90a2717", "openfda": {"upc": ["0041220721702"], "unii": ["G63QQF2NOX", "V06SV4M95S", "4X49Y0596W", "5A68WGF6WM"], "spl_set_id": ["d6184ba2-0e47-459a-8777-1f27be2140a6"], "manufacturer_name": ["H.E.B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 TUBE (37808-914-12)", "package_ndc": "37808-914-12", "marketing_start_date": "20190205"}], "brand_name": "H.E.B ULTRA", "product_id": "37808-914_c6b84cf6-4361-5352-e053-2995a90a2717", "dosage_form": "AEROSOL, SPRAY", "product_ndc": "37808-914", "generic_name": "SPF 50 Sunscreen", "labeler_name": "H.E.B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "H.E.B ULTRA", "active_ingredients": [{"name": "AVOBENZONE", "strength": "30 mg/mL"}, {"name": "HOMOSALATE", "strength": "100 mg/mL"}, {"name": "OCTISALATE", "strength": "45 mg/mL"}, {"name": "OCTOCRYLENE", "strength": "80 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190205", "listing_expiration_date": "20261231"}