Ban
- Product NDC
- 10596-336
- 11-digit product format
- 105960336
- Labeler code
- 10596
- Product ID
- 10596-336_21d96f55-985d-b309-e063-6394a90a97ba
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Chlorohydrate
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Kao USA Inc.
- Application
- M019
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2012-01-01
- Substance
- ALUMINUM CHLOROHYDRATE
- Active strength
- 20 g/103mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ban
- Brand name suffix
- Roll-On Antiperspirant Deodorant Regular
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALUMINUM CHLOROHYDRATE | 20 g/103mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | HPN8MZW13M |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10596-336-14 | BanRoll-On Antiperspirant Deodorant Regular | 4 in 1 PACKAGE | LIQUID | 4 | | 14 |
| 10596-336-14 | BanRoll-On Antiperspirant Deodorant Regular | 103 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 103 | | 14 |
| 10596-336-15 | BanRoll-On Antiperspirant Deodorant Regular | 44 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 44 | | 14 |
| 10596-336-35 | BanRoll-On Antiperspirant Deodorant Regular | 103 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 103 | | 14 |
| 10596-336-70 | BanRoll-On Antiperspirant Deodorant Regular | 2 in 1 PACKAGE | LIQUID | 2 | | 14 |
| 10596-336-70 | BanRoll-On Antiperspirant Deodorant Regular | 103 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 103 | | 14 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10596-336 | BAN ROLL-ON ANTIPERSPIRANT DEODORANT REGULAR (ALUMINUM CHLOROHYDRATE) LIQUID [KAO USA INC.] | 14 | Current NDC, Legacy NDC, 6 package rows | 20240913_1f76588b-e2ea-43b5-ae07-29e290df001d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 10596-336-14 | 10596033614 | 4 BOTTLE, WITH APPLICATOR in 1 PACKAGE (10596-336-14) / 103 mL in 1 BOTTLE, WITH APPLICATOR | | 2019-12-12 | 0000-00-00 | No | No | Current |
| 10596-336-15 | 10596033615 | 44 mL in 1 BOTTLE, WITH APPLICATOR (10596-336-15) | 44 ml | 2016-11-04 | 0000-00-00 | No | No | Current |
| 10596-336-35 | 10596033635 | 103 mL in 1 BOTTLE, WITH APPLICATOR (10596-336-35) | 103 ml | 2012-01-01 | 0000-00-00 | No | No | Current |
| 10596-336-70 | 10596033670 | 2 BOTTLE, WITH APPLICATOR in 1 PACKAGE (10596-336-70) / 103 mL in 1 BOTTLE, WITH APPLICATOR | | 2016-09-12 | 0000-00-00 | No | No | Current |