MyDerm Aloe and Lidocaine
- Product NDC
- 53329-037
- 11-digit product format
- 533290037
- Labeler code
- 53329
- Product ID
- 53329-037_52bef461-4f91-2f1e-e063-6394a90aa0cd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Medline Industries
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-02-26
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- .5 g/100mL
- 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
- MyDerm Aloe and Lidocaine
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LIDOCAINE HYDROCHLORIDE | .5 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V13007Z41A |
| Rxcui | 1011849 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53329-037-09 | MyDerm Aloe and Lidocaine | 592 mL in 1 BOTTLE, PLASTIC | GEL | 592 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 53329-037-09 | 53329003709 | 592 mL in 1 BOTTLE, PLASTIC (53329-037-09) | 592 ml | 2019-02-26 | No | No | Historical |