HANNA HAND SANITIZER gel
- Product NDC
- 71193-101
- 11-digit product format
- 711930101
- Labeler code
- 71193
- Product ID
- 71193-101_ae6217ac-7b64-0c9d-e053-2a95a90aa11e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Rainbow Beauty Cosmetic Co., Ltd.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-09-03
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 70 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 71193-101-01 | HANNA HAND SANITIZER gel | 500 mL in 1 BOTTLE | GEL | 500 | | 1 |
| 71193-101-02 | HANNA HAND SANITIZER gel | 300 mL in 1 BOTTLE | GEL | 300 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71193-101 | HANNA HAND SANITIZER GEL (ALCOHOL) GEL [RAINBOW BEAUTY COSMETIC CO., LTD.] | 1 | Legacy NDC, 2 package rows | 20200903_ae622d94-36ae-38b5-e053-2995a90a0a22.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 |
|---|
| 71193-101-01 | 71193010101 | 500 mL in 1 BOTTLE (71193-101-01) | 500 ml | 2020-09-03 | 0000-00-00 | No | No | Current |
| 71193-101-02 | 71193010102 | 300 mL in 1 BOTTLE (71193-101-02) | 300 ml | 2020-09-03 | 0000-00-00 | No | No | Current |