Hand Sanitizer
- Product NDC
- 50814-050
- 11-digit product format
- 508140050
- Labeler code
- 50814
- Product ID
- 50814-050_a40b9643-51ac-30c2-e053-2a95a90abc20
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- GFA Production (Xiamen) Co., Ltd.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-01
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 1 mL/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50814-050 | HAND SANITIZER (ALCOHOL) GEL [GFA PRODUCTION (XIAMEN) CO., LTD.] | 3 | Legacy NDC | 20241011_9dd76719-03d8-4dae-8049-262ce31032fd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50814-050-02 | 50814005002 | 200 mL in 1 BOTTLE (50814-050-02) | 200 ml | 2020-03-01 | 0000-00-00 | No | No | Current |