Softlips
- Product NDC
- 10742-7011
- 11-digit product format
- 107427011
- Labeler code
- 10742
- Product ID
- 10742-7011_2978d002-ed43-0525-e063-6394a90a982f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- dimethicone, octinoxate, octisalate, oxybenzone
- Dosage form
- KIT
- Labeler
- The Mentholatum Company
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2017-01-02
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Softlips
- Brand name suffix
- Pearl Plus Vanilla
- Listing expiration
- 2026-12-31
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10742-7011-1 | SoftlipsPearl Plus Vanilla | 1 in 1 PACKAGE | KIT | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10742-7011 | SOFTLIPS PEARL PLUS VANILLA (DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE) KIT [THE MENTHOLATUM COMPANY] | 3 | Current NDC, Legacy NDC, 1 package rows | 20241219_107bcaa9-4347-4979-be44-35183a9ee67e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 10742-7011-1 | 10742701101 | 1 KIT in 1 PACKAGE (10742-7011-1) * 2 g in 1 CYLINDER * 2 g in 1 CYLINDER | 1 kit | 2017-01-02 | 0000-00-00 | No | No | Current |