Hand Sanitizer, Glitter Fever
- Product NDC
- 72866-009
- 11-digit product format
- 728660009
- Labeler code
- 72866
- Product ID
- 72866-009_eea07c75-2fed-2cae-e053-2a95a90a08b0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Merci Handy Corporation
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-01
- Marketing end
- 2025-06-30
- Substance
- ALCOHOL
- Active strength
- 670 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 72866-009 | HAND SANITIZER, GLITTER FEVER (ALCOHOL) GEL [MERCI HANDY CORPORATION] | 4 | Legacy NDC | 20221130_957c51c2-ab0b-4785-bba7-6f4f83e38dae.zip |
| 72866-009 | MAGIC POUCH (ALCOHOL) KIT [MERCI HANDY CORPORATION] | 2 | Legacy NDC | 20221130_b232f228-3f85-a75a-e053-2a95a90a691b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72866-009-30 | 72866000930 | 30 mL in 1 BOTTLE (72866-009-30) | 30 ml | 2020-03-10 | 0000-00-00 | No | No | Current |