Lightning X Sting and Bite Relief Pads
- Product NDC
- 59050-416
- 11-digit product format
- 590500416
- Labeler code
- 59050
- Product ID
- 59050-416_518698c0-a1af-760f-e063-6394a90a5160
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzocaine, Isopropyl Alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Changzhou Maokang Medical Products Co., Ltd.
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-05-11
- Substance
- BENZOCAINE; ISOPROPYL ALCOHOL
- Active strength
- 60; 600 mg/mL; mg/mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lightning X Sting and Bite Relief Pads
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOCAINE | 60 mg/mL |
| ISOPROPYL ALCOHOL | 600 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U3RSY48JW5, ND2M416302 |
| Rxcui | 895749 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59050-416-01 | Lightning X Sting and Bite Relief Pads | 0.4 mL in 1 POUCH | LIQUID | 0.4 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 59050-416-01 | 59050041601 | .4 mL in 1 POUCH (59050-416-01) | 2026-05-11 | No | No | Current |