MELLOW HAND SANITIZER (ORIGINAL)
- Product NDC
- 50154-022
- 11-digit product format
- 501540022
- Labeler code
- 50154
- Product ID
- 50154-022_4b292d5b-79ed-4b0e-8254-a75b2eba235b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Lantern Enterprises Ltd.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-06-16
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 62 mL/100mL
- 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 |
|---|
| 50154-022-01 | MELLOW HAND SANITIZER (ORIGINAL)WITH MOISTURIZER AND VITAMIN E | 59 mL in 1 BOTTLE | GEL | 59 | | 1 |
| 50154-022-02 | MELLOW HAND SANITIZER (ORIGINAL)WITH MOISTURIZER AND VITAMIN E | 236 mL in 1 BOTTLE | GEL | 236 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50154-022 | MELLOW HAND SANITIZER (ORIGINAL) WITH MOISTURIZER AND VITAMIN E (ALCOHOL) GEL [LANTERN ENTERPRISES LTD.] | 1 | Legacy NDC, 2 package rows | 20170616_5f8949e8-a15f-4aaa-9690-7c7caa538be7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50154-022-01 | 50154002201 | 59 mL in 1 BOTTLE (50154-022-01) | 59 ml | 2017-06-16 | 0000-00-00 | No | No | Current |
| 50154-022-02 | 50154002202 | 236 mL in 1 BOTTLE (50154-022-02) | 236 ml | 2017-06-16 | 0000-00-00 | No | No | Current |