Octinoxate
- Product NDC
- 60541-8407
- 11-digit product format
- 605418407
- Labeler code
- 60541
- Product ID
- 60541-8407_332c5fb6-263c-4b12-b37b-59a80c19c71e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Hayden Caleel LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2013-09-01
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE
- Active strength
- 0 g/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 60541-8407-4 | Octinoxate | 30 mL in 1 BOTTLE | LOTION | 30 | | 2 |
| 60541-8407-4 | Octinoxate | 1 in 1 BOX | LOTION | 1 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60541-8407 | OCTINOXATE LOTION [HAYDEN CALEEL LLC] | 2 | Legacy NDC, 2 package rows | 20150522_3a4e17fb-22c8-4c79-a140-17000ff13802.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 60541-8407-4 | 60541840704 | 30 mL in 1 BOTTLE | 30 ml | Historical |