Dr.Jart Every Sun Day Sun Fluid SPF 30
- Product NDC
- 49404-129
- 11-digit product format
- 494040129
- Labeler code
- 49404
- Product ID
- 49404-129_3f08263a-352c-67ca-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Have & Be Co., Ltd.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2016-01-25
- Marketing end
- 0000-00-00
- Substance
- HOMOSALATE; OCTOCRYLENE; OCTISALATE; AVOBENZONE
- Active strength
- 10 mg/100mL; mg/100mL; mg/100mL; mg/100mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record