Hanzol
- Product NDC
- 76917-074
- 11-digit product format
- 769170074
- Labeler code
- 76917
- Product ID
- 76917-074_2478b4f6-9139-41cd-b7f8-27af921d2034
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Plymouth Technology, Inc.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-05-11
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 70 L/100L
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 76917-074-01 | HanzolGelled Hand Sanitizer | 3.8 L in 1 JUG | GEL | 3.8 | | 1 |
| 76917-074-05 | HanzolGelled Hand Sanitizer | 18.9 L in 1 CONTAINER | GEL | 18.9 | | 1 |
| 76917-074-55 | HanzolGelled Hand Sanitizer | 208.2 L in 1 DRUM | GEL | 208.2 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76917-074 | HANZOL GELLED HAND SANITIZER (ETHYL ALCOHOL) GEL [PLYMOUTH TECHNOLOGY, INC.] | 1 | Legacy NDC, 3 package rows | 20200527_0918346f-9202-40ee-8a2c-762597f5f1f1.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 |
|---|
| 76917-074-01 | 76917007401 | 3.8 L in 1 JUG (76917-074-01) | 3.8 l | 2020-05-11 | 0000-00-00 | No | No | Current |
| 76917-074-05 | 76917007405 | 18.9 L in 1 CONTAINER (76917-074-05) | 18.9 l | 2020-05-11 | 0000-00-00 | No | No | Current |
| 76917-074-55 | 76917007455 | 208.2 L in 1 DRUM (76917-074-55) | 208.2 l | 2020-05-11 | 0000-00-00 | No | No | Current |