DR.JART EVERY SUN DAY SUN FLUID 29 mg/mL
homosalate, octinoxate, octisalate, octocrylene, avobenzone · LIQUID · Have & Be Co., Ltd.
DR.JART EVERY SUN DAY SUN FLUID is a liquid containing homosalate, octinoxate, octisalate, octocrylene, avobenzone at 29 mg/mL, taken topical. Manufactured by Have & Be Co., Ltd..
Key Facts
- Brand Name
- DR.JART EVERY SUN DAY SUN FLUID
- Generic Name
- homosalate, octinoxate, octisalate, octocrylene, avobenzone
- NDC Code (Product)
49404-307- Manufacturer
- Have & Be Co., Ltd.
- Strength
- 29 mg/mL
- Dosage Form
- LIQUID
- Route
- TOPICAL
- Marketing Status
- Application #
- M020
- Marketing Start
- 08/11/2023
Recall History
No Recall HistoryFrequently Asked Questions
What is DR.JART EVERY SUN DAY SUN FLUID used for?
DR.JART EVERY SUN DAY SUN FLUID contains homosalate, octinoxate, octisalate, octocrylene, avobenzone. It is a liquid taken topical. Consult your doctor for specific uses.
Is DR.JART EVERY SUN DAY SUN FLUID a controlled substance?
DR.JART EVERY SUN DAY SUN FLUID is not classified as a controlled substance by the DEA.
What is the generic name for DR.JART EVERY SUN DAY SUN FLUID?
The generic name for DR.JART EVERY SUN DAY SUN FLUID is homosalate, octinoxate, octisalate, octocrylene, avobenzone. There are no other listed brand versions of homosalate, octinoxate, octisalate, octocrylene, avobenzone.
What is the NDC code for DR.JART EVERY SUN DAY SUN FLUID 29 mg/mL?
The NDC (National Drug Code) for DR.JART EVERY SUN DAY SUN FLUID 29 mg/mL is 49404-307, listed by Have & Be Co., Ltd..
Other DR.JART EVERY SUN DAY SUN FLUID Dosages
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)