NDC 76162-253-04 - Topcare Complete Lice Treatment Kit
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 76162-253
- Requested NDC
- 76162-253-04
- Package NDCs from labels
- 76162-253-04, 76162-253-08
- Manufacturer
- Topco Associates, LLC | Weeks & Leo Co., Inc. | WEEKS & LEO COMPANY, INC.
- Effective date
- 2025-11-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Topcare Lice Treatment Kit | Topco Associates, LLC | Weeks & Leo Co., Inc. | WEEKS & LEO COMPANY, INC. | 2025-11-11 | HUMAN OTC DRUG LABEL |
| Topcare Lice Killing Shampoo | Topco Associates, LLC | Weeks & Leo Co., Inc. | 2023-12-06 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 76162-253-04 | Topcare Complete Lice Treatment Kit | 118 mL in 1 BOTTLE | SHAMPOO | 118 mL | 4 g in 100mL | 3 |
| 76162-253-08 | Topcare Lice Killing | 236 mL in 1 BOTTLE | SHAMPOO | 236 | 1 | |
| 76162-253-08 | Topcare Lice Killing | 1 in 1 CARTON | SHAMPOO | 1 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 76162-253 | TOPCARE COMPLETE LICE TREATMENT KIT (PIPERONYL BUTOXIDE, PYRETHRUM EXTRACT) KIT [TOPCO ASSOCIATES, LLC] | 2 | Current NDC | 20250109_0bf3980f-d10d-afc9-e063-6294a90acbf5.zip |
| 76162-253 | TOPCARE LICE KILLING (PIPERONYL BUTOXIDE, PYRETHRUM EXTRACT) SHAMPOO [TOPCO ASSOCIATES, LLC] | 1 | Current NDC, 2 package rows | 20231207_0be04816-e173-8046-e063-6294a90acdb6.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.