8.75oz ANTIBACTERIAL FOAM HANDSOAP - OCEAN BREEZE
- Product NDC
- 90114-253
- 11-digit product format
- 901140253
- Labeler code
- 90114
- Product ID
- 90114-253_b5b4d785-b4df-ceb0-e053-2a95a90ab412
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Hero Brands, Inc.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-11-05
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 90114-253-01 | 8.75oz ANTIBACTERIAL FOAM HANDSOAP - OCEAN BREEZE | 259 mL in 1 BOTTLE | GEL | 259 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 90114-253 | 8.75OZ ANTIBACTERIAL FOAM HANDSOAP - OCEAN BREEZE (BENZALKONIUM CHLORIDE) GEL [HERO BRANDS, INC.] | 1 | Legacy NDC, 1 package rows | 20201205_b5b4c13c-211d-5226-e053-2995a90ae6e3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 90114-253-01 | 90114025301 | 259 mL in 1 BOTTLE (90114-253-01) | 259 ml | 2020-11-05 | 0000-00-00 | No | No | Current |