BZK Antiseptic Swab
- Product NDC
- 73288-003
- 11-digit product format
- 732880003
- Labeler code
- 73288
- Product ID
- 73288-003_483a3158-c2a7-9f42-e063-6294a90a1dc4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- NINGBO TIANBO FIRST AID PRODUCT CO., LTD.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-08-29
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- .4 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BZK Antiseptic Swab
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BENZALKONIUM CHLORIDE | .4 g/100mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| F5UM2KM3W7 | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1038561 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 94043f4e-fe47-4b6f-8354-30697daaed81 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| fb7ab793-2c12-4079-b100-a64f73bef25a | Product name | 4 | 20240712 |
| b0cbf770-6cc3-4aa4-9158-755110c2b9f7 | Product name | 2 | 20230717 |
| dc7c5daa-021f-40dd-b00d-63982cb2067a | Product name | 1 | 20230426 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 5 | 20200925 |
| 816b97af-edc5-4060-aff1-b814bdbcad50 | Product name | 1 | 20190415 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| 419aab54-5d5a-4146-9453-026d4a9991be | Product name | 2 | 20170525 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 2 | 20160823 |
| 89dac932-b90a-4410-9ab1-84c53e57de25 | Product name | 1 | 20150316 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73288-003-01 | BZK Antiseptic Swab | 2 in 1 PACKAGE | SOLUTION | 2 | 6 | |
| 73288-003-01 | BZK Antiseptic Swab | 0.85 mL in 1 PACKET | SOLUTION | 0.85 | 6 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Anti-Fungal Powder | MICONAZOLE NITRATE | TopCo Associates | 19c3fbc5-abde-57df-e063-6394a90a125c | 2025-11-06 | Warnings | M005 |
| Tolnaftate | FOOT ODOR CONTROL SPRAY | Topco Associates LLC | 17993a9f-0d44-43a1-8608-94ee8a08b539 | 2025-11-06 | Warnings | M005 |
| DVO Estriol cream | ESTRIOL0.2% | Guangzhou Huixue Biotechnology Co., Ltd. | 42e4cc84-7c00-6937-e063-6294a90a0c09 | 2025-11-05 | Warnings | M005 |
| Medline | MICONAZOL NITRATE | Medline Industries, LP | dad58efb-cc20-577a-e053-2a95a90abd9d | 2025-11-03 | Warnings | M005 |
| Tolnafate | TOLNAFTATE POWDER SPRAY | HEB | c6af941a-0b85-4611-a6f3-b13fcf3c4a87 | 2025-11-03 | Warnings | M005 |
| Tolnaftate | FOOT ODOR CONTROL SPRAY | HEB | c585605b-ecb8-4dd8-9205-a9be02d751fa | 2025-11-03 | Warnings | M005 |
| Premier Solutions Antifungal Tolnaftate Liquid | TOLNAFTATE | Premier Brands of America, Inc. | e1971c1c-5687-577b-e053-2a95a90ad95f | 2025-11-03 | Warnings | M005 |
| Miconazole nitrate | ANTIFUNGAL MICONAZOLE LIQUID CONTINUOUS SPRAY | Premier Brands of America Inc. | 3803c643-35d1-06d4-e063-6294a90ac6f6 | 2025-11-03 | Warnings | M005 |
| Anti-fungal Powder Miconazole Nitrate | MICONAZOLE NITRATE | Meijer Distribution Inc | 03fd069d-685d-b8ac-e063-6394a90a31f8 | 2025-10-31 | Warnings | M005 |
| Tolnaftate | ANTIFUNGAL LIQUID SPRAY | Premier Brands of America Inc. | 7a6a63cd-e87d-4229-8acf-b65d63909eb6 | 2025-10-31 | Warnings | M005 |
| Azolen | MICONAZOLE NITRATE | Stratus Pharmaceuticals, Inc. | 9c2574f3-3be4-405a-9c87-943dc6ef8777 | 2025-10-30 | Warnings | M005 |
| Family Care Antifungal | CLOTRIMAZOLE | United Exchange Corp. | 63255079-ecf1-1e77-e053-2a91aa0a7b6c | 2025-10-30 | Warnings | M005 |
| Miconazorb AF | MICONAZOLE NITRATE | AmerisourceBergen Drug Corporation | 13a20d21-42d5-fe56-e063-6394a90aaf57 | 2025-10-30 | Warnings | M005 |
| Antifungal Liquid Continuous | MICONAZOLE NITRATE | Family Dollar Services, Inc | 17cc4601-f946-df8b-e063-6394a90a3897 | 2025-10-30 | Warnings | M005 |
| Tolnaftate | ANTIFUNGAL LIQUID SPRAY | ARMY & AIR FORCE EXCHANGE SERVICE | 932b1be8-3dbb-49ae-822a-c44a24fbe36a | 2025-10-30 | Warnings | M005 |
| Miconazole nitrate | ANTIFUNGAL MICONAZOLE LIQUID CONTINUOUS SPRAY | GEISS, DESTIN AND DUNN, INC. | c367c2e8-5423-bf01-e053-2a95a90ab8e9 | 2025-10-30 | Warnings | M005 |
| Miconazole Nitrate | JOCK ITCH SPRAY | Harris Teeter, LLC | 636b0d6f-4e36-4c96-9e71-7bfdebb7f3cb | 2025-10-30 | Warnings | M005 |
| Tolnaftate | ANTIFUNGAL LIQUID SPRAY | Harris Teeter, LLC | f140e9bb-507b-4048-8b7b-8cc51b6a497d | 2025-10-30 | Warnings | M005 |
| HEB Athlete Foot Antifungal | MICONAZOLE NITRATE | HEB | 2e204111-b5d3-0220-e063-6294a90a67bb | 2025-10-30 | Warnings | M005 |
| Tolnaftate | ANTIFUNGAL SPRAY LIQUID | Kroger Co. | 0cfebac3-684d-4599-b75f-9a82708db717 | 2025-10-30 | Warnings | M005 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1038561 | benzalkonium Cl 0.4 % Medicated Pad | PSN | 94043f4e-fe47-4b6f-8354-30697daaed81 | 6 |
| 1038561 | benzalkonium chloride 4 MG/ML Medicated Pad | SCD | 94043f4e-fe47-4b6f-8354-30697daaed81 | 6 |
| 1038561 | benzalkonium chloride 0.4 % Medicated Towelette | SY | 94043f4e-fe47-4b6f-8354-30697daaed81 | 6 |
| 1038561 | benzalkonium chloride 0.4 % Topical Swab | SY | 94043f4e-fe47-4b6f-8354-30697daaed81 | 6 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 73288-003-01 | 73288000301 | 2 PACKET in 1 PACKAGE (73288-003-01) / .85 mL in 1 PACKET | 2 packet | 2019-08-29 | 0000-00-00 | No | No | Current |