Aegis Daily Facial
- Product NDC
- 71690-201
- 11-digit product format
- 716900201
- Labeler code
- 71690
- Product ID
- 71690-201_3fa98c98-03ae-4c00-beb7-3b0b49f46a78
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, and OCTOCRYLENE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- JNTLee Inc. dba Panacea
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-10-20
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 29 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71690-201-01 | Aegis Daily Facial SPF 25 | 1 in 1 CARTON | LOTION | 1 | | 1 |
| 71690-201-50 | Aegis Daily Facial SPF 25 | 50 mL in 1 BOTTLE, PUMP | LOTION | 50 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71690-201 | AEGIS DAILY FACIAL SPF 25 (AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, AND OCTOCRYLENE) LOTION [JNTLEE INC. DBA PANACEA] | 1 | Legacy NDC, 2 package rows | 20171020_4f09bc31-96d9-4aee-bc87-fcaa86af70dc.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71690-201-01 | 71690020101 | 1 BOTTLE, PUMP in 1 CARTON (71690-201-01) > 50 mL in 1 BOTTLE, PUMP (71690-201-50) | | 2017-10-20 | 0000-00-00 | No | No | Current |
| 71690-201-50 | 71690020150 | 50 mL in 1 BOTTLE, PUMP | 50 ml | | | | | Historical |