DT Collagen
- Product NDC
- 70522-001
- 11-digit product format
- 705220001
- Labeler code
- 70522
- Product ID
- 70522-001_6067f927-ac01-500b-e053-2a91aa0ae1cf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octocrylene
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- DT Collagen, Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2016-01-01
- Marketing end
- 0000-00-00
- Substance
- HOMOSALATE; OCTOCRYLENE; OCTINOXATE; OCTISALATE; AVOBENZONE
- Active strength
- 10 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70522-001-01 | DT Collagen | 50 mL in 1 TUBE | CREAM | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70522-001 | DT COLLAGEN (OCTOCRYLENE) CREAM [DT COLLAGEN, INC.] | 2 | Legacy NDC, 1 package rows | 20171216_2883b764-0d58-57ad-e054-00144ff88e88.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70522-001-01 | 70522000101 | 50 mL in 1 TUBE (70522-001-01) | 50 ml | 2016-01-01 | 0000-00-00 | No | No | Current |