Package 83108-100-00

Brand: luminosity activation day edition

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 83108-100-00
Digits Only 8310810000
Product NDC 83108-100
Description

1 KIT in 1 KIT (83108-100-00) * 3 mL in 1 BOTTLE (83108-001-13)

Marketing

Marketing Status
Discontinued 2026-09-01
Brand luminosity activation day edition
Generic zinc oxide
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "450e0206-d7d4-bd87-e063-6394a90a3c3e", "openfda": {"upc": ["9359782003978"], "spl_set_id": ["ba026282-38a6-4dd3-aa5a-fb6d215accc1"], "manufacturer_name": ["Rationale Group Pty Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (83108-100-00)  *  3 mL in 1 BOTTLE (83108-001-13)", "package_ndc": "83108-100-00", "marketing_end_date": "20260901", "marketing_start_date": "20231115"}], "brand_name": "Luminosity Activation Day Edition", "product_id": "83108-100_450e0206-d7d4-bd87-e063-6394a90a3c3e", "dosage_form": "KIT", "product_ndc": "83108-100", "generic_name": "ZINC OXIDE", "labeler_name": "Rationale Group Pty Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Luminosity Activation Day Edition", "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260901", "marketing_start_date": "20231115"}