Lidocaine HCI
- Product NDC
- 73352-204
- 11-digit product format
- 733520204
- Labeler code
- 73352
- Product ID
- 73352-204_47f7f06b-720f-eeec-e063-6294a90ae823
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine HCI
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Trifluent Pharma, LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-09
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 40 mg/g
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lidocaine HCI
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LIDOCAINE HYDROCHLORIDE | 40 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V13007Z41A |
| Rxcui | 1010895 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73352-204-60 | Lidocaine HCI | 30 g in 1 TUBE | CREAM | 30 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 73352-204-60 | 73352020460 | 30 g in 1 TUBE (73352-204-60) | 30 g | 2026-01-09 | No | No | Historical |