SUNBAR SPF 15
- Product NDC
- 63550-810
- 11-digit product format
- 635500810
- Labeler code
- 63550
- Product ID
- 63550-810_e20e5f13-95b4-4bfc-9b95-44533d0c533f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE HOMOSALATE OCTISALATE OXYBENZONE
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Kamins Dermatologics Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2010-09-30
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OXYBENZONE
- Active strength
- 30 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63550-810-12 | SUNBAR SPF 15 | 150 mL in 1 BOX | SPRAY | 150 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63550-810 | SUNBAR SPF 15 (AVOBENZONE HOMOSALATE OCTISALATE OXYBENZONE) SPRAY [KAMINS DERMATOLOGICS INC.] | 1 | Legacy NDC, 1 package rows | 20101007_38053dac-a26a-41a4-8bbb-7bc094c99d93.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 63550-810-12 | 63550081012 | 150 mL in 1 BOX | 150 ml | Historical |