Complexion Protection Moisturizer SPF
- Product NDC
- 70809-1902
- Requested package NDC
- 70809-1902-1
- 11-digit product format
- 708091902
- Labeler code
- 70809
- Product ID
- 70809-1902_b349f645-31f5-b202-e053-2995a90a46e5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- benzophenone, avobenzone, octinoxate, octisalate cream
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- USRX LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-07-08
- Marketing end
- 0000-00-00
- Substance
- OCTISALATE; OCTINOXATE; AVOBENZONE; BENZOPHENONE
- Active strength
- 5 mg/100mL; mg/100mL; mg/100mL; mg/100mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70809-1902-1 | Complexion Protection Moisturizer SPF | 50 mL in 1 TUBE | CREAM | 50 | | 7 |
| 70809-1902-2 | Complexion Protection Moisturizer SPF | 12 mL in 1 TUBE | CREAM | 12 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70809-1902 | COMPLEXION PROTECTION MOISTURIZER SPF (BENZOPHENONE, AVOBENZONE, OCTINOXATE, OCTISALATE CREAM) CREAM [USRX LLC] | 7 | Legacy NDC, 2 package rows | 20241004_8d343fec-85a7-613b-e053-2a95a90a4a78.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70809-1902-1 | 70809190201 | 50 mL in 1 TUBE (70809-1902-1) | 50 ml | 2019-07-08 | 0000-00-00 | No | No | Current |