Antiperspirant ODABAN
- Product NDC
- 84724-0001
- 11-digit product format
- 847240001
- Labeler code
- 84724
- Product ID
- 84724-0001_4601fa40-e8f3-d162-e063-6294a90a55d9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Spray Antiperspirant ODABAN
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Archifox GmbH & Co. KG
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2024-09-01
- Substance
- ALUMINUM CHLORIDE
- Active strength
- 4.35 mg/30mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Antiperspirant ODABAN
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALUMINUM CHLORIDE | 4.35 mg/30mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3CYT62D3GA |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84724-0001-1 | Antiperspirant ODABAN | 30 mL in 1 BOTTLE, SPRAY | SPRAY | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 84724-0001 | ANTIPERSPIRANT ODABAN (SPRAY ANTIPERSPIRANT ODABAN) SPRAY [ARCHIFOX GMBH & CO. KG] | 2 | Current NDC, 1 package rows | 20241008_21c81851-0966-5a43-e063-6294a90a211c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84724-0001-1 | 84724000101 | 30 mL in 1 BOTTLE, SPRAY (84724-0001-1) | 30 ml | 2024-09-01 | No | No | Historical |