Mellow Instant Hand Sanitizer Original
- Product NDC
- 50154-0040
- 11-digit product format
- 501540040
- Labeler code
- 50154
- Product ID
- 50154-0040_08259087-acd2-49ab-a4a6-d9121d545481
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Lantern Enterprises Ltd.
- Application
- part333
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2009-12-30
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 62 mL/100mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 50154-0040-6 | Mellow Instant Hand Sanitizer Original | 59 mL in 1 BOTTLE | GEL | 59 | | 1 |
| 50154-0040-7 | Mellow Instant Hand Sanitizer Original | 236 mL in 1 BOTTLE | GEL | 236 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50154-0040 | MELLOW INSTANT HAND SANITIZER ORIGINAL (ETHYL ALCOHOL) GEL [LANTERN ENTERPRISES LTD.] | 1 | Legacy NDC, 2 package rows | 20091231_7f399c03-d00f-4327-a485-e5114af5b8f0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 50154-0040-6 | 50154004006 | 59 mL in 1 BOTTLE | 59 ml | Historical |
| 50154-0040-7 | 50154004007 | 236 mL in 1 BOTTLE | 236 ml | Historical |