Daily Defense
- Product NDC
- 68726-265
- 11-digit product format
- 687260265
- Labeler code
- 68726
- Product ID
- 68726-265_f0d03d57-bc22-ee5b-e053-2a95a90ab23a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Face Sunscreen
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- CP Skin Health Group, Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-05-01
- Marketing end
- 0000-00-00
- Substance
- OCTISALATE; OCTOCRYLENE; ZINC OXIDE
- Active strength
- 5 g/100mL; g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68726-265 | DAILY DEFENSE SPF 50 (FACE SUNSCREEN) LOTION [CP SKIN HEALTH GROUP, INC.] | 6 | Legacy NDC | 20240215_b7b5bfb2-996a-1b3e-e053-2a95a90a976c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68726-265-11 | 68726026511 | 50 mL in 1 TUBE (68726-265-11) | 50 ml | 2020-05-01 | 0000-00-00 | No | No | Current |
| 68726-265-37 | 68726026537 | 7.4 mL in 1 TUBE (68726-265-37) | 7.4 ml | 2020-05-01 | 0000-00-00 | No | No | Current |