Package 67879-309-51

Brand: sun therape face and body spf-35

Generic: avobenzone, octinoxate, octisalate, oxybenzone
NDC Package

Package Facts

Identity

Package NDC 67879-309-51
Digits Only 6787930951
Product NDC 67879-309
Description

1 TUBE in 1 BOX (67879-309-51) / 125 mL in 1 TUBE (67879-309-12)

Marketing

Marketing Status
Marketed Since 2016-06-10
Brand sun therape face and body spf-35
Generic avobenzone, octinoxate, octisalate, oxybenzone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "1f947bfc-53ab-1cbe-e063-6294a90aebb1", "openfda": {"unii": ["G63QQF2NOX", "4Y5P7MUD51", "4X49Y0596W", "95OOS7VE0Y"], "spl_set_id": ["6a96623f-c37c-4e67-925e-f133461d726d"], "manufacturer_name": ["PHARMAGEL INTERNATIONAL INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (67879-309-51)  / 125 mL in 1 TUBE (67879-309-12)", "package_ndc": "67879-309-51", "marketing_start_date": "20160610"}], "brand_name": "SUN THERAPE FACE AND BODY SPF-35", "product_id": "67879-309_1f947bfc-53ab-1cbe-e063-6294a90aebb1", "dosage_form": "LOTION", "product_ndc": "67879-309", "generic_name": "AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE", "labeler_name": "PHARMAGEL INTERNATIONAL INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SUN THERAPE FACE AND BODY", "brand_name_suffix": "SPF-35", "active_ingredients": [{"name": "AVOBENZONE", "strength": "3 g/100mL"}, {"name": "OCTINOXATE", "strength": "7.5 g/100mL"}, {"name": "OCTISALATE", "strength": "5 g/100mL"}, {"name": "OXYBENZONE", "strength": "3 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150618", "listing_expiration_date": "20261231"}