Ocean Breeze Scented Hand Sanitizer
- Product NDC
- 33992-1205
- 11-digit product format
- 339921205
- Labeler code
- 33992
- Product ID
- 33992-1205_b1865156-6016-410e-b580-43c6eafd9620
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Greenbrier International
- Application
- part333E
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-03-15
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 62 mL/100mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 33992-1205-1 | Ocean Breeze Scented Hand Sanitizer | 29 mL in 1 BOTTLE | GEL | 29 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 33992-1205 | OCEAN BREEZE SCENTED HAND SANITIZER (ALCOHOL) GEL [GREENBRIER INTERNATIONAL] | 1 | Legacy NDC, 1 package rows | 20120316_adc3949f-13cf-421f-ab87-901dc3d08cdd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 33992-1205-1 | 33992120501 | 29 mL in 1 BOTTLE | 29 ml | Historical |