PIXI SUN MIST SPF 30
- Product NDC
- 70686-101
- 11-digit product format
- 706860101
- Labeler code
- 70686
- Product ID
- 70686-101_fc9615cf-17f0-47dd-b79b-f32206b8708a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AMILOXATE, OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- PIXI, INC
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2016-08-03
- Marketing end
- 0000-00-00
- Substance
- AMILOXATE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE
- Active strength
- 3 g/100mL; g/100mL; g/100mL; g/100mL
- 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 |
|---|
| 70686-101-13 | PIXI SUN MIST SPF 30 | 80 mL in 1 BOTTLE, SPRAY | SPRAY | 80 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70686-101 | PIXI SUN MIST SPF 30 (AMILOXATE, OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE) SPRAY [PIXI, INC] | 2 | Legacy NDC, 1 package rows | 20181109_49001a18-ae05-493e-92da-95b56401b323.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 70686-101-13 | 70686010113 | 80 mL in 1 BOTTLE, SPRAY | 80 ml | Historical |