Betadine Foam Cleanser
- Product NDC
- 67618-184
- 11-digit product format
- 676180184
- Labeler code
- 67618
- Product ID
- 67618-184_1fcb644d-8c46-4f10-aff1-f0b5fa74eba3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Atlantis Consumer Healthcare, Inc.
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-02-01
- 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
- Betadine Foam Cleanser
- 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 |
| Rxcui | 1046593 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67618-184-08 | Betadine Foam Cleanser | 237 mL in 1 BOTTLE | AEROSOL, FOAM | 237 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67618-184-08 | 67618018408 | 237 mL in 1 BOTTLE (67618-184-08) | 237 ml | 2026-02-01 | No | No | Current |