AGE DEFYING MOISTURIZER
- Product NDC
- 46007-202
- Requested package NDC
- 46007-202-12
- 11-digit product format
- 460070202
- Labeler code
- 46007
- Product ID
- 46007-202_d53e0ec1-2b75-48c5-e053-2a95a90aba3e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Skin Authority LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-04-19
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE
- Active strength
- 2 g/100mL; g/100mL; g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 46007-202-12 | AGE DEFYING MOISTURIZERSPF 18 | 50 mL in 1 BOTTLE | LOTION | 50 | | 9 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 46007-202 | AGE DEFYING MOISTURIZER SPF 18 (AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE) LOTION [SKIN AUTHORITY LLC] | 8 | Legacy NDC, 1 package rows | 20250110_20e16afe-95b3-4f47-8dd0-cf9c6eecb42f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 46007-202-12 | 46007020212 | 50 mL in 1 BOTTLE (46007-202-12) | 50 ml | 2012-04-19 | 0000-00-00 | No | No | Current |