XTRA
- Product NDC
- 84987-001
- 11-digit product format
- 849870001
- Labeler code
- 84987
- Product ID
- 84987-001_2fb7059d-5d89-3836-e063-6394a90a976c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Zhejiang Jifu Daily Chemical Co., Ltd.
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-11-27
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- .13 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- XTRA
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | .13 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84987-001-01 | XTRA | 399 mL in 1 BOTTLE, SPRAY | SPRAY | 399 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 84987-001 | XTRA (BENZALKONIUM CHLORIDE) SPRAY [ZHEJIANG JIFU DAILY CHEMICAL CO., LTD.] | 2 | Current NDC, 1 package rows | 20250309_27df3fce-3958-d4ea-e063-6394a90a1785.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84987-001-01 | 84987000101 | 399 mL in 1 BOTTLE, SPRAY (84987-001-01) | 399 ml | 2024-11-27 | No | No | Current |