Package 67879-308-51

Brand: derma brite spf 35

Generic: octinoxate, octisalate, oxybenzone
NDC Package

Package 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
Marketed Since 2016-06-13
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"}