luminosity activation day edition
Generic: zinc oxide
Labeler: rationale group pty ltdDrug Facts
Product Profile
Brand Name
luminosity activation day edition
Generic Name
zinc oxide
Labeler
rationale group pty ltd
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
83108-100
Product ID
83108-100_450e0206-d7d4-bd87-e063-6394a90a3c3e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Marketing Start
2023-11-15
Marketing End
2026-09-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83108100
Hyphenated Format
83108-100
Supplemental Identifiers
UPC
Packaging Origin
Original Packager
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
luminosity activation day edition (source: ndc)
Generic Name
zinc oxide (source: ndc)
Application Number
M020 (source: ndc)
Resolved Composition
Strengths
- 24 %
Packaging
- 1 KIT in 1 KIT (83108-100-00) * 3 mL in 1 BOTTLE (83108-001-13)
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
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"}