NDC 10107-429-01 - Herb Street Anti-Itch Stick
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
- 10107-429
- Requested NDC
- 10107-429-01
- Package NDCs from labels
- 10107-429-01, 10107-429-02
- Manufacturer
- Balassa Laboratories Inc.
- Effective date
- 2024-10-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Herb Street Anti-Itch Stick | Balassa Laboratories Inc. | 2024-10-01 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10107-429-01 | Herb Street Anti-Itch Stick | 16.8 g in 1 TUBE | STICK | 16.8 | 2 | |
| 10107-429-02 | Herb Street Anti-Itch Stick | 1 in 1 CARTON | STICK | 1 | 2 |
DailyMed Dashboard NDC Coverage#
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.
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| FREEZE IT Menthol | MENTHOL | LiquidCapsule Manufacturing LLC | de8d8007-5718-4fb4-a8c6-4650d2ca9c8f | 2025-06-05 | Warnings | M017 |
| HEEL PAIN Relief Gel Roll-On | MENTHOL | Guangzhou Zhupuyou E-commerce Co., Ltd | 36bacb5f-c1af-2e97-e063-6394a90afe5c | 2025-06-04 | Warnings | M017 |
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| HealthWise Lidocaine and Menthol | LIDOCAINE AND MENTHOL | Veridian Healthcare | 36c27642-f913-1aad-e063-6294a90a4343 | 2025-06-04 | Warnings | M017 |
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| Burn | LIDOCAINE HYDROCHLORIDE | J&A Digital Inc. | d4b09055-b93e-466f-9e24-cae098af6e24 | 2025-06-02 | Warnings | M017 |
| RE-LEVE | MENTHOL | SOMBRA COSMETICS INC. | b4b39d79-0439-41e7-adca-e5ccb8f44e40 | 2025-05-29 | Warnings | M017 |
| PAIN NO MORE THERAPY | MENTHOL CAMPHOR | SOMBRA COSMETICS INC. | f7bacc8e-6a8b-4cd8-bd0e-68890bee5818 | 2025-05-29 | Warnings | M017 |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.