TRACELESS
- Product NDC
- 59158-731
- 11-digit product format
- 591580731
- Labeler code
- 59158
- Product ID
- 59158-731_292b6d23-8e51-4a64-964c-cf1b49b45530
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- PRESCRIPTIVES INC.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2001-06-01
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE
- Active strength
- 2 mL/100mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 59158-731-01 | TRACELESSSKIN RESPONSIVE TINT | 1 in 1 CARTON | CREAM | 1 | | 2 |
| 59158-731-02 | TRACELESSSKIN RESPONSIVE TINT | 30 mL in 1 TUBE | CREAM | 30 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59158-731 | TRACELESS SKIN RESPONSIVE TINT (OCTINOXATE) CREAM [PRESCRIPTIVES INC.] | 2 | Legacy NDC, 2 package rows | 20110407_783bad5b-8cf4-4c23-92b5-bda2181328d1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 59158-731-01 | 59158073101 | 1 in 1 CARTON | | Historical |
| 59158-731-02 | 59158073102 | 30 mL in 1 TUBE | 30 ml | Historical |