Package 85491-205-04

Brand: solar eclipse extreme sunscreen

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 85491-205-04
Digits Only 8549120504
Product NDC 85491-205
Description

113 g in 1 BOTTLE, PUMP (85491-205-04)

Marketing

Marketing Status
Marketed Since 2025-05-14
Brand solar eclipse extreme sunscreen
Generic zinc oxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4614829b-e8c2-c720-e063-6394a90ac40a", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["36bfa691-48c0-8033-e063-6294a90ad899"], "manufacturer_name": ["ULTRAVIOLET SKINCARE LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "113 g in 1 BOTTLE, PUMP (85491-205-04)", "package_ndc": "85491-205-04", "marketing_start_date": "20250514"}], "brand_name": "Solar Eclipse Extreme Sunscreen", "product_id": "85491-205_4614829b-e8c2-c720-e063-6394a90ac40a", "dosage_form": "CREAM", "product_ndc": "85491-205", "generic_name": "Zinc Oxide", "labeler_name": "ULTRAVIOLET SKINCARE LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Solar Eclipse Extreme Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "200 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250514", "listing_expiration_date": "20261231"}