Ocean Breeze Scented Antibacterial Hand Sanitizer
- Product NDC
- 80684-005
- 11-digit product format
- 806840005
- Labeler code
- 80684
- Product ID
- 80684-005_08a026b8-bede-ca5b-e063-6294a90a0b4e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Fourstar Group USA, Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-11-07
- Substance
- ALCOHOL
- Active strength
- .7 mL/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ocean Breeze Scented Antibacterial Hand Sanitizer
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | .7 mL/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 581662 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 80684-005-01 | Ocean Breeze Scented Antibacterial Hand Sanitizer | 29 mL in 1 BOTTLE | GEL | 29 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80684-005 | OCEAN BREEZE SCENTED ANTIBACTERIAL HAND SANITIZER (ALCOHOL) GEL [FOURSTAR GROUP USA, INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231102_b3391b8e-877f-e74a-e053-2995a90afd62.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 |
|---|
| 80684-005-01 | 80684000501 | 29 mL in 1 BOTTLE (80684-005-01) | 29 ml | 2020-11-07 | 0000-00-00 | No | No | Current |