ULTRASOL
- Product NDC
- 59886-352
- 11-digit product format
- 598860352
- Labeler code
- 59886
- Product ID
- 59886-352_27f9ee8c-31fd-4c97-8209-c521eb2e4d1e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octinoxate, Octisalate, Octocrylene, Oxybenzone
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- Fischer Pharmaceuticals Ltd
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-06-10
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
- Active strength
- 3 g/100g; g/100g; g/100g; g/100g; g/100g; g/100g
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 59886-352-66 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-23bc-f424-e053-dadaa90a57ce | Dr. Fischer ULTRASOL Sunscreen Spray Lotion SPF45 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59886-352-66 | ULTRASOLSunscreen SPF45 | 200 g in 1 CAN | AEROSOL, SPRAY | 200 | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 59886-352 | ULTRASOL SUNSCREEN SPF45 (AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) AEROSOL, SPRAY [FISCHER PHARMACEUTICALS LTD] | 2 | Legacy NDC, 1 package rows | 20100610_a33c156d-0904-42b9-bc04-157559c7fe00.zip |
Packages#
| Package NDC | 11-digit format | Description | Units | Status |
|---|---|---|---|---|
| 59886-352-66 | 59886035266 | 200 g in 1 CAN | 200 g | Historical |