Package 81568-101-50
Brand: dr. brandt sun shield spf 50
Generic: zinc oxidePackage 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
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"}