Bactine Max Dry
- Product NDC
- 65197-815
- 11-digit product format
- 651970815
- Labeler code
- 65197
- Product ID
- 65197-815_144bf707-6b26-4386-a0ba-0a4a3a797be9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- lidocaine hydrochloride
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- WellSpring Pharmaceutical Corporation
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-01-31
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 4 g/100g
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Bactine Max Dry
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LIDOCAINE HYDROCHLORIDE | 4 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V13007Z41A |
| Rxcui | 1869797 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 65197-815-04 | Bactine Max Dry | 113 g in 1 CAN | SPRAY | 113 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65197-815 | BACTINE MAX DRY (LIDOCAINE HYDROCHLORIDE) SPRAY [WELLSPRING PHARMACEUTICAL CORPORATION] | 6 | Current NDC, 1 package rows | 20250110_466404cd-c46a-4944-b1ac-3b3b17f436a1.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 |
|---|
| 65197-815-04 | 65197081504 | 113 g in 1 CAN (65197-815-04) | 113 g | 2023-01-31 | No | No | Current |