Package 83656-2106-2

Brand: blume sunburst sunscreen

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 83656-2106-2
Digits Only 8365621062
Product NDC 83656-2106
Product ID 83656-2106_4134b186-b3a0-a307-e063-6394a90a223a
Description

1 BOTTLE in 1 CARTON (83656-2106-2) / 50 mL in 1 BOTTLE (83656-2106-1)

Marketing

Marketing Status
Marketed Since 2024-03-01
Brand blume sunburst sunscreen
Generic zinc oxide
Sample Package No

Linked Drug Pages (1)

Blume Sunburst Sunscreen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4134b186-b3a0-a307-e063-6394a90a223a", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["21ef2c6b-8ae7-8bcf-e063-6294a90ae9e1"], "manufacturer_name": ["Blume"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (83656-2106-2)  / 50 mL in 1 BOTTLE (83656-2106-1)", "package_ndc": "83656-2106-2", "marketing_start_date": "20240301"}], "brand_name": "Blume Sunburst Sunscreen", "product_id": "83656-2106_4134b186-b3a0-a307-e063-6394a90a223a", "dosage_form": "LOTION", "product_ndc": "83656-2106", "generic_name": "Zinc Oxide", "labeler_name": "Blume", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Blume Sunburst Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "132 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240301", "listing_expiration_date": "20261231"}