Package 81568-101-50

Brand: dr. brandt sun shield spf 50

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 81568-101-50
Digits Only 8156810150
Product NDC 81568-101
Description

1 BOTTLE, DROPPER in 1 BOX (81568-101-50) / 50 mL in 1 BOTTLE, DROPPER

Marketing

Marketing Status
Marketed Since 2021-02-15
Brand dr. brandt sun shield spf 50
Generic zinc oxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "d6922659-fdc4-48c0-a7d6-a3051be051c1", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["6f8af59b-d423-4250-8ddc-061fea886e3e"], "manufacturer_name": ["Dr. Brandt"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 BOX (81568-101-50)  / 50 mL in 1 BOTTLE, DROPPER", "package_ndc": "81568-101-50", "marketing_start_date": "20210215"}], "brand_name": "dr. brandt SUN SHIELD SPF 50", "product_id": "81568-101_d6922659-fdc4-48c0-a7d6-a3051be051c1", "dosage_form": "LIQUID", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "81568-101", "generic_name": "Zinc Oxide", "labeler_name": "Dr. Brandt", "product_type": "HUMAN OTC DRUG", "brand_name_base": "dr. brandt SUN SHIELD SPF 50", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "17 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210215", "listing_expiration_date": "20261231"}