Luminosity Activation Day Edition
ZINC OXIDE · KIT · Rationale Group Pty Ltd
No Recall History
Plain English
Luminosity Activation Day Edition is a kit containing zinc oxide. Manufactured by Rationale Group Pty Ltd.
Key Facts
- Brand Name
- Luminosity Activation Day Edition
- Generic Name
- ZINC OXIDE
- NDC Code (Product)
83108-100- Manufacturer
- Rationale Group Pty Ltd
- Dosage Form
- KIT
- Marketing Status
- Application #
- M020
- Marketing Start
- 11/15/2023
Recall History
No Recall HistoryFrequently Asked Questions
What is Luminosity Activation Day Edition used for?
Luminosity Activation Day Edition contains ZINC OXIDE. It is a kit taken as directed. Consult your doctor for specific uses.
Is Luminosity Activation Day Edition a controlled substance?
Luminosity Activation Day Edition is not classified as a controlled substance by the DEA.
What is the generic name for Luminosity Activation Day Edition?
The generic name for Luminosity Activation Day Edition is ZINC OXIDE. There are 12 other brand versions of ZINC OXIDE.
What is the NDC code for Luminosity Activation Day Edition ?
The NDC (National Drug Code) for Luminosity Activation Day Edition is 83108-100, listed by Rationale Group Pty Ltd.
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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)