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United States · US · US:83108-100_450e0206-d7d4-bd87-e063-6394a90a3c3e
Luminosity Activation Day Edition
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRationale Group Pty Ltd
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1183108100001 KIT in 1 KIT (83108-100-00) * 3 mL in 1 BOTTLE (83108-001-13)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": null,
"spl_meta": {
"ba026282-38a6-4dd3-aa5a-fb6d215accc1": {
"match": "brand_token",
"title": "LUMINOSITY ACTIVATION DAY EDITION (ZINC OXIDE) KIT [RATIONALE GROUP PTY LTD]",
"spl_version": "3",
"published_date": "2025-12-04"
}
},
"productid": "83108-100_450e0206-d7d4-bd87-e063-6394a90a3c3e",
"productndc": "83108-100",
"dosage_form": "KIT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": null,
"proprietary_name": "Luminosity Activation Day Edition",
"active_ingred_unit": null,
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "ZINC OXIDE",
"start_marketing_date": "20231115",
"active_numerator_strength": null
}Access this data programmatically
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