ultra violette velvet screen blurring mineral skinscreen

Generic: spf50

Labeler: wild child laboratories pty ltd
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name ultra violette velvet screen blurring mineral skinscreen
Generic Name spf50
Labeler wild child laboratories pty ltd
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

zinc oxide 22.75 g/100mL

Manufacturer
Wild Child Laboratories PTY Ltd

Identifiers & Regulatory

Product NDC 30807-1060
Product ID 30807-1060_47b74894-0916-f792-e063-6394a90aeb22
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2027-12-31
Marketing Start 2024-12-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 308071060
Hyphenated Format 30807-1060

Supplemental Identifiers

UNII
SOI2LOH54Z

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ultra violette velvet screen blurring mineral skinscreen (source: ndc)
Generic Name spf50 (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 22.75 g/100mL
source: ndc
Packaging
  • 15 mL in 1 TUBE (30807-1060-1)
  • 50 mL in 1 TUBE (30807-1060-2)
source: ndc

Packages (2)

30807-1060-1 15 mL in 1 TUBE (30807-1060-1) 30807-1060-2 50 mL in 1 TUBE (30807-1060-2)

Ingredients (1)

zinc oxide (22.75 g/100mL)

Linked Drug Pages (1)

ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN ndc-match (0.9)

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"}