Handy Andys
- Product NDC
- 78299-141
- 11-digit product format
- 782990141
- Labeler code
- 78299
- Product ID
- 78299-141_d68d27fa-25f6-3ef8-e053-2a95a90adb53
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hand Sanitizer Spray
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- LXR Biotech LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-05-01
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 80 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 78299-141-11 | Handy Andys | 57 mL in 1 BOTTLE | LIQUID | 57 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 78299-141 | HANDY ANDYS (HAND SANITIZER SPRAY) LIQUID [LXR BIOTECH LLC] | 1 | Legacy NDC, 1 package rows | 20200915_af491c8f-645e-65c7-e053-2a95a90a7dce.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 |
|---|
| 78299-141-11 | 78299014111 | 57 mL in 1 BOTTLE (78299-141-11) | 57 ml | 2020-09-12 | 0000-00-00 | No | No | Current |
| 78299-141-12 | 78299014112 | 57 mL in 1 BOTTLE (78299-141-12) | 57 ml | 2020-09-12 | 0000-00-00 | No | No | Current |