AB 3000
- Product NDC
- 63039-1006
- 11-digit product format
- 630391006
- Labeler code
- 63039
- Product ID
- 63039-1006_34a08384-3cb2-4aad-a03f-f4107d725d8f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Chemco
- Application
- M
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-12-29
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- .13 kg/100kg
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- AB 3000
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | .13 kg/100kg |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
| Rxcui | 1046593 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63039-1006-1 | AB 3000 | 3.80564 kg in 1 BOTTLE, PLASTIC | LIQUID | 3.80564 | | 9 |
| 63039-1006-2 | AB 3000 | 1 in 1 BOX | LIQUID | 1 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63039-1006 | AB 3000 (BENZALKONIUM CHLORIDE) LIQUID [CHEMCO] | 8 | Current NDC, Legacy NDC, 2 package rows | 20241212_892c8911-9f1a-4c0c-9106-6d9a90d577a9.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 |
|---|
| 63039-1006-1 | 63039100601 | 3.80564 kg in 1 BOTTLE, PLASTIC | 3.80564 kg | | | | | Historical |
| 63039-1006-2 | 63039100602 | 1 BOTTLE, PLASTIC in 1 BOX (63039-1006-2) / 3.80564 kg in 1 BOTTLE, PLASTIC (63039-1006-1) | | 2020-12-29 | 0000-00-00 | No | No | Current |