Hand Sanitizer
- Product NDC
- 69394-001
- 11-digit product format
- 693940001
- Labeler code
- 69394
- Product ID
- 69394-001_e4a2adc1-fcf5-895a-e053-2a95a90ac09b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- AAkron Rule Corporation
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-08-04
- 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
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 |
|---|
| 69394-001-01 | Hand Sanitizer | 30 mL in 1 BOTTLE, PLASTIC | LIQUID | 30 | | 4 |
| 69394-001-02 | Hand Sanitizer | 89 mL in 1 BOTTLE, PLASTIC | LIQUID | 89 | | 4 |
| 69394-001-03 | Hand Sanitizer | 1893 mL in 1 BOTTLE, PLASTIC | LIQUID | 1893 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69394-001 | HAND SANITIZER (ALCOHOL) LIQUID [AAKRON RULE CORPORATION] | 4 | Legacy NDC, 3 package rows | 20220726_7ff1c2d4-3a11-4606-829e-0c8930d7c3e2.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 |
|---|
| 69394-001-01 | 69394000101 | 30 mL in 1 BOTTLE, PLASTIC (69394-001-01) | 30 ml | 2020-08-04 | 0000-00-00 | No | No | Current |
| 69394-001-02 | 69394000102 | 89 mL in 1 BOTTLE, PLASTIC (69394-001-02) | 89 ml | 2020-08-04 | 0000-00-00 | No | No | Current |
| 69394-001-03 | 69394000103 | 1893 mL in 1 BOTTLE, PLASTIC (69394-001-03) | 1893 ml | 2020-08-04 | 0000-00-00 | No | No | Current |