DAY L
- Product NDC
- 63550-122
- 11-digit product format
- 635500122
- Labeler code
- 63550
- Product ID
- 63550-122_eeca4350-d0b9-5f00-e053-2995a90a2751
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE OCTISALATE OCTINOXATE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Kamins Dermatologics Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2004-03-01
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; OCTINOXATE; OCTISALATE
- Active strength
- 25 mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63550-122-03 | 63550012203 | 50 mL in 1 BOX (63550-122-03) | 50 ml | 2004-03-01 | 0000-00-00 | No | No | Current |