Package 67879-308-51
Brand: derma brite spf 35
Generic: octinoxate, octisalate, oxybenzonePackage Facts
Identity
Package NDC
67879-308-51
Digits Only
6787930851
Product NDC
67879-308
Description
1 JAR in 1 BOX (67879-308-51) / 56 g in 1 JAR (67879-308-11)
Marketing
Marketing Status
Brand
derma brite spf 35
Generic
octinoxate, octisalate, oxybenzone
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "1f945a92-b7d2-59f2-e063-6394a90a2483", "openfda": {"unii": ["4Y5P7MUD51", "4X49Y0596W", "95OOS7VE0Y"], "spl_set_id": ["fe10912e-00e3-406c-a80c-d9c991dc9f8b"], "manufacturer_name": ["PHARMAGEL INTERNATIONAL INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 JAR in 1 BOX (67879-308-51) / 56 g in 1 JAR (67879-308-11)", "package_ndc": "67879-308-51", "marketing_start_date": "20160613"}], "brand_name": "DERMA BRITE SPF 35", "product_id": "67879-308_1f945a92-b7d2-59f2-e063-6394a90a2483", "dosage_form": "CREAM", "product_ndc": "67879-308", "generic_name": "OCTINOXATE, OCTISALATE, OXYBENZONE", "labeler_name": "PHARMAGEL INTERNATIONAL INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DERMA BRITE", "brand_name_suffix": "SPF 35", "active_ingredients": [{"name": "OCTINOXATE", "strength": "7.5 g/100g"}, {"name": "OCTISALATE", "strength": "5 g/100g"}, {"name": "OXYBENZONE", "strength": "3 g/100g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150618", "listing_expiration_date": "20261231"}