Package 30807-1060-2

Brand: ultra violette velvet screen blurring mineral skinscreen

Generic: spf50
NDC Package

Package Facts

Identity

Package NDC 30807-1060-2
Digits Only 3080710602
Product NDC 30807-1060
Description

50 mL in 1 TUBE (30807-1060-2)

Marketing

Marketing Status
Marketed Since 2024-12-01
Brand ultra violette velvet screen blurring mineral skinscreen
Generic spf50
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "47b74894-0916-f792-e063-6394a90aeb22", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["2767ba3e-7434-d474-e063-6294a90aa4ff"], "manufacturer_name": ["Wild Child Laboratories PTY Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 mL in 1 TUBE (30807-1060-1)", "package_ndc": "30807-1060-1", "marketing_start_date": "20241201"}, {"sample": false, "description": "50 mL in 1 TUBE (30807-1060-2)", "package_ndc": "30807-1060-2", "marketing_start_date": "20241201"}], "brand_name": "ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN", "product_id": "30807-1060_47b74894-0916-f792-e063-6394a90aeb22", "dosage_form": "CREAM", "product_ndc": "30807-1060", "generic_name": "SPF50", "labeler_name": "Wild Child Laboratories PTY Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "22.75 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241201", "listing_expiration_date": "20271231"}