Pacific Blue Ultra Foaming
- Product NDC
- 54622-701
- 11-digit product format
- 546220701
- Labeler code
- 54622
- Product ID
- 54622-701_4a0396f3-a0ee-da8e-e063-6294a90a1c93
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Georgia-Pacific Consumer Products LP
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2016-06-02
- Substance
- ALCOHOL
- Active strength
- 70 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pacific Blue Ultra Foaming
- Brand name suffix
- Fragrance Free
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 70 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 54622-701-01 | Pacific Blue Ultra FoamingFragrance Free | 1000 mL in 1 BOTTLE, DISPENSING | SOLUTION | 1000 | | 19 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 54622-701 | PACIFIC BLUE ULTRA FOAMING FRAGRANCE FREE (ETHYL ALCOHOL) SOLUTION [GEORGIA-PACIFIC CONSUMER PRODUCTS LP] | 17 | Current NDC, Legacy NDC, 1 package rows | 20240929_0bdc1b9a-0a56-466b-ac51-95c499e90978.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 54622-701-01 | 54622070101 | 1000 mL in 1 BOTTLE, DISPENSING (54622-701-01) | 1000 ml | 2016-06-09 | 0000-00-00 | No | No | Current |