Hand Sanitizer Soothing Gel
- Product NDC
- 61354-010
- 11-digit product format
- 613540010
- Labeler code
- 61354
- Product ID
- 61354-010_a798ac0d-30af-3714-e053-2a95a90a3836
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- OXYGEN DEVELOPMENT, LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-06-08
- 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 |
|---|
| 61354-010-01 | Hand Sanitizer Soothing Gel | 925 mL in 1 BOTTLE, PUMP | LIQUID | 925 | | 1 |
| 61354-010-02 | Hand Sanitizer Soothing Gel | 148 mL in 1 BOTTLE | LIQUID | 148 | | 1 |
| 61354-010-03 | Hand Sanitizer Soothing Gel | 55 mL in 1 BOTTLE | LIQUID | 55 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61354-010 | HAND SANITIZER SOOTHING GEL (ALCOHOL) LIQUID [OXYGEN DEVELOPMENT, LLC] | 1 | Legacy NDC, 3 package rows | 20200609_a798ac0d-30bd-3714-e053-2a95a90a3836.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61354-010-01 | 61354001001 | 925 mL in 1 BOTTLE, PUMP (61354-010-01) | 925 ml | 2020-06-08 | 0000-00-00 | No | No | Current |
| 61354-010-02 | 61354001002 | 148 mL in 1 BOTTLE (61354-010-02) | 148 ml | 2020-06-08 | 0000-00-00 | No | No | Current |
| 61354-010-03 | 61354001003 | 55 mL in 1 BOTTLE (61354-010-03) | 55 ml | 2020-06-08 | 0000-00-00 | No | No | Current |