NYX Professional Makeup Buttermelt Glaze SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30 73 mg/mL
Homosalate,Octisalate and Octocrylene · CREAM · LOreal USA Products Inc
NYX Professional Makeup Buttermelt Glaze SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30 is a cream containing homosalate,octisalate and octocrylene at 73 mg/mL, taken topical. Manufactured by LOreal USA Products Inc.
Key Facts
- Brand Name
- NYX Professional Makeup Buttermelt Glaze SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30
- Generic Name
- Homosalate,Octisalate and Octocrylene
- NDC Code (Product)
49967-356- Manufacturer
- LOreal USA Products Inc
- Strength
- 73 mg/mL
- Dosage Form
- CREAM
- Route
- TOPICAL
- Marketing Status
- Application #
- M020
- Marketing Start
- 01/10/2024
Recall History
No Recall HistoryFrequently Asked Questions
What is NYX Professional Makeup Buttermelt Glaze SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30 used for?
NYX Professional Makeup Buttermelt Glaze SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30 contains Homosalate,Octisalate and Octocrylene. It is a cream taken topical. Consult your doctor for specific uses.
Is NYX Professional Makeup Buttermelt Glaze SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30 a controlled substance?
NYX Professional Makeup Buttermelt Glaze SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30 is not classified as a controlled substance by the DEA.
What is the generic name for NYX Professional Makeup Buttermelt Glaze SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30?
The generic name for NYX Professional Makeup Buttermelt Glaze SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30 is Homosalate,Octisalate and Octocrylene. There are no other listed brand versions of Homosalate,Octisalate and Octocrylene.
What is the NDC code for NYX Professional Makeup Buttermelt Glaze SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30 73 mg/mL?
The NDC (National Drug Code) for NYX Professional Makeup Buttermelt Glaze SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30 73 mg/mL is 49967-356, listed by LOreal USA Products Inc.
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)