Lidotral 3.88% Roll on
- Product NDC
- 59088-307
- 11-digit product format
- 590880307
- Labeler code
- 59088
- Product ID
- 59088-307_db1085fe-0a1e-c4cc-e053-2a95a90aa838
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine HCI
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- PureTek Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2024-02-28
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 38.8 mg/g
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| V13007Z41A | LIDOCAINE HYDROCHLORIDE | 6108-05-0 | LIDOCAINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 59088-307-07 | 59088030707 | 85 g in 1 BOTTLE (59088-307-07) | 85 g | 2024-02-28 | No | No | Historical |