Lidozall
- Product NDC
- 72835-004
- 11-digit product format
- 728350004
- Labeler code
- 72835
- Product ID
- 72835-004_436cebe5-b978-2a2f-e063-6294a90a7227
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- LIDOCAINE HYDROCHLORIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- V2 Pharma LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-11-21
- 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
- Lidozall
- 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 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72835-004-01 | Lidozall | 2 g in 1 PACKET | CREAM | 2 | | 4 |
| 72835-004-20 | Lidozall | 20 in 1 CARTON | CREAM | 20 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72835-004 | LIDOZALL (LIDOCAINE HYDROCHLORIDE) CREAM [V2 PHARMA LLC] | 1 | Current NDC, 2 package rows | 20241220_1eb2dfb2-3ad1-488b-aed9-17220e34a10c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72835-004-01 | 72835000401 | 2 g in 1 PACKET | 2 g | | | | Historical |
| 72835-004-20 | 72835000420 | 20 PACKET in 1 CARTON (72835-004-20) / 2 g in 1 PACKET (72835-004-01) | 20 packet | 2024-12-16 | No | No | Current |