Rapidol
- Product NDC
- 55758-440
- 11-digit product format
- 557580440
- Labeler code
- 55758
- Product ID
- 55758-440_43d00a9a-fb44-69c9-e063-6394a90adc7e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Pharmadel LLC
- Application
- M004
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-11-04
- Substance
- BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
- Active strength
- 400; 3.5; 5000 [USP'U]/g; mg/g; [USP'U]/g
- Pharmacologic classes
- Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS], Decreased Cell Wall Synthesis & Repair [PE], Polymyxin-class Antibacterial [EPC], Polymyxins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Rapidol
- Brand name suffix
- Triple Antibiotic
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BACITRACIN ZINC | 400 [USP'U]/g |
| NEOMYCIN SULFATE | 3.5 mg/g |
| POLYMYXIN B SULFATE | 5000 [USP'U]/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 89Y4M234ES, 057Y626693, 19371312D4 |
| Rxcui | 204602 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55758-440-02 | RapidolTriple Antibiotic | 1 in 1 CARTON | OINTMENT | 1 | | 5 |
| 55758-440-02 | RapidolTriple Antibiotic | 56 g in 1 TUBE | OINTMENT | 56 | | 5 |
| 55758-440-03 | RapidolTriple Antibiotic | 1 in 1 CARTON | OINTMENT | 1 | | 5 |
| 55758-440-03 | RapidolTriple Antibiotic | 57 g in 1 TUBE | OINTMENT | 57 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55758-440 | RAPIDOL TRIPLE ANTIBIOTIC (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE) OINTMENT [PHARMADEL LLC] | 3 | Current NDC, 4 package rows | 20241105_1ad22205-f8c3-b142-e063-6394a90a0044.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 55758-440-02 | 55758044002 | 1 in 1 CARTON | | | | | Historical |
| 55758-440-03 | 55758044003 | 1 TUBE in 1 CARTON (55758-440-03) / 57 g in 1 TUBE | 1 tube | 2026-01-01 | No | No | Current |