Package 70764-201-52

Brand: botanical soothing spf-30

Generic: octinoxate, octisalate, zinc oxide
NDC Package

Package Facts

Identity

Package NDC 70764-201-52
Digits Only 7076420152
Product NDC 70764-201
Description

1 BOTTLE in 1 BOX (70764-201-52) / 74 mL in 1 BOTTLE (70764-201-22)

Marketing

Marketing Status
Marketed Since 2016-06-08
Brand botanical soothing spf-30
Generic octinoxate, octisalate, zinc oxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "474bb04f-2be5-2dd9-e063-6394a90a6a3c", "openfda": {"unii": ["4Y5P7MUD51", "4X49Y0596W", "SOI2LOH54Z"], "spl_set_id": ["00a923fe-e6da-420e-a705-4773ecc2176b"], "manufacturer_name": ["CONTROL CORRECTIVE SKINCARE INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 BOX (70764-201-52)  / 74 mL in 1 BOTTLE (70764-201-22)", "package_ndc": "70764-201-52", "marketing_start_date": "20160608"}], "brand_name": "BOTANICAL SOOTHING SPF-30", "product_id": "70764-201_474bb04f-2be5-2dd9-e063-6394a90a6a3c", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "70764-201", "generic_name": "OCTINOXATE, OCTISALATE, ZINC OXIDE", "labeler_name": "CONTROL CORRECTIVE SKINCARE INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BOTANICAL SOOTHING", "brand_name_suffix": "SPF-30", "active_ingredients": [{"name": "OCTINOXATE", "strength": "6.9 g/100mL"}, {"name": "OCTISALATE", "strength": "3 g/100mL"}, {"name": "ZINC OXIDE", "strength": "4 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160608", "listing_expiration_date": "20261231"}