NDC 10157-9409 - Blistex Baby Kanka
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
- 10157-9409
- Package NDCs from labels
- 10157-9409-1
- Manufacturer
- Blistex Inc.
- Effective date
- 2015-01-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Blistex Baby Kanka ® Gel | Blistex Inc. | 2015-01-22 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 10157-9409-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-dd11-f424-e053-dadaa90a57ce | Blistex Baby Kanka ® Gel |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10157-9409-1 | Blistex Baby Kanka | 10 g in 1 TUBE | GEL | 10 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 10157-9409 | BLISTEX BABY KANKA (BENZOCAINE) GEL [BLISTEX INC.] | 1 | 1 package rows | 20150129_b70ff808-43d3-4a14-867e-b56f9db9da87.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Benzocaine | ACTIVE INGREDIENT | U3RSY48JW5 | BLISTEX BABY KANKA (BENZOCAINE) GEL [BLISTEX INC.] | 1 | |
| Benzocaine | ACTIVE MOIETY | U3RSY48JW5 | BLISTEX BABY KANKA (BENZOCAINE) GEL [BLISTEX INC.] | 1 | |
| GLYCERIN | INACTIVE INGREDIENT | PDC6A3C0OX | BLISTEX BABY KANKA (BENZOCAINE) GEL [BLISTEX INC.] | 1 | |
| METHYLPARABEN | INACTIVE INGREDIENT | A2I8C7HI9T | BLISTEX BABY KANKA (BENZOCAINE) GEL [BLISTEX INC.] | 1 | |
| POLYETHYLENE GLYCOL 3350 | INACTIVE INGREDIENT | G2M7P15E5P | BLISTEX BABY KANKA (BENZOCAINE) GEL [BLISTEX INC.] | 1 | |
| POLYETHYLENE GLYCOL 400 | INACTIVE INGREDIENT | B697894SGQ | BLISTEX BABY KANKA (BENZOCAINE) GEL [BLISTEX INC.] | 1 | |
| PROPYLPARABEN | INACTIVE INGREDIENT | Z8IX2SC1OH | BLISTEX BABY KANKA (BENZOCAINE) GEL [BLISTEX INC.] | 1 | |
| SORBIC ACID | INACTIVE INGREDIENT | X045WJ989B | BLISTEX BABY KANKA (BENZOCAINE) GEL [BLISTEX INC.] | 1 | |
| SUCRALOSE | INACTIVE INGREDIENT | 96K6UQ3ZD4 | BLISTEX BABY KANKA (BENZOCAINE) GEL [BLISTEX INC.] | 1 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| HurriCaine Topical Anesthetic | BENZOCAINE | Beutlich Pharmaceuticals LLC | 723da3ae-3f1f-4962-920b-f2a30c8c3253 | 2025-01-08 | Warnings, Adverse reactions | U3RSY48JW5 |
| Sting Relief Swab | BENZOCAINE | Epic Medical Supply Corp | 259fbfe4-d67c-ea1e-e063-6294a90a0fb0 | 2025-01-07 | Warnings | U3RSY48JW5 |
| Benzo-Jel | BENZOCAINE | Henry Schein Inc. | bc2e7ac3-f9e4-49cc-9f0c-6fe94479314d | 2025-01-03 | Warnings | U3RSY48JW5 |
| Benzo-Jel | BENZOCAINE | Henry Schein Inc. | fb38b10d-0faf-403c-9921-d4f6b0f6aa55 | 2025-01-03 | Warnings | U3RSY48JW5 |
| Benzo-Jel | BENZOCAINE | Henry Schein Inc. | a9dc2245-c029-4453-bfc5-8fb899873c34 | 2025-01-03 | Warnings | U3RSY48JW5 |
| Benzo-Jel | BENZOCAINE | Henry Schein Inc. | ba49a18d-8568-421b-a495-8fee863c9757 | 2025-01-03 | Warnings | U3RSY48JW5 |
| Benzo-Jel | BENZOCAINE | Henry Schein Inc. | c9b584d9-7407-445a-b084-926250af9f8e | 2025-01-03 | Warnings | U3RSY48JW5 |
| Benzo-Jel | BENZOCAINE | Henry Schein Inc. | 4aa6eec8-394a-4ecb-8173-66561fd64913 | 2025-01-03 | Warnings | U3RSY48JW5 |
| Benzo-Jel | BENZOCAINE | Henry Schein Inc. | 25c99ae3-90f4-4a63-924d-f810b3ba6e60 | 2025-01-03 | Warnings | U3RSY48JW5 |
| Benzo-Jel | BENZOCAINE | Henry Schein Inc. | 84e8d5c8-2a35-4179-9a9c-9a4a52c2cae6 | 2025-01-03 | Warnings | U3RSY48JW5 |
| Prevention Oncology Mouth Rinse | GLYCERIN | Prevention Health Sciences, Inc. | 1ec9ed1c-bcb6-3a0a-e054-00144ff8d46c | 2025-01-01 | Warnings | PDC6A3C0OX |
| CLENZIDERM THERAPEUTIC MOISTURIZER | GLYCERIN | Obagi Cosmeceuticals LLC | d60e22e3-831e-4787-a82c-e7763c287553 | 2025-01-01 | Warnings | PDC6A3C0OX |
| Rite Aid Hydration Lubricant Eye Drops | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Rite Aid Corporation | ecac1351-e944-21da-e053-2995a90a6d34 | 2024-12-31 | Warnings | B697894SGQ |
| Tucks Triple Relief Hemorrhoidal | WHITE PETROLATUM, GLYCERIN, PRAMOXINE HYDROCHLORIDE, AND PHENYLEPHRINE HYDROCHLORIDE | Blistex Inc. | bf892e90-2d9b-4fa0-8ee4-8a2736be6c30 | 2024-12-24 | Warnings | PDC6A3C0OX |
| BiteMD External Analgesic First Aid Antiseptic | BENZOCAINE, CAMPHOR (SYNTHETIC), AND PHENOL | United Industries Corporation | 4c60db03-6d2b-4ae0-a200-718b3a50eb0f | 2024-12-23 | Warnings | U3RSY48JW5 |
| Glitch Advanced Relief Eye Drops | POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL | Misemer Pharmaceutical, Inc | 03778509-3374-2168-e063-6294a90a9505 | 2024-12-23 | Warnings | B697894SGQ |
| Pedia-Lax | GLYCERIN | C.B. Fleet Company, Inc. | 4e15f6ca-a40c-485f-be3f-07c2ed7cb498 | 2024-12-23 | Warnings | PDC6A3C0OX |
| OASIS Tears Preservative-Free Lubricant Eye | GLYCERIN | OASIS Medical, Inc. | d9d71b1d-82a6-42e7-9ef2-2d041daef936 | 2024-12-23 | Warnings | PDC6A3C0OX |
| Household Antigens | ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, BUTYL ACETATE, ETHYL ACETATE, TOLUENE, XYLENE, BISPHENOL A, PETROLEUM, FORMALINUM, GLYPHOSATE, METHYLPARABEN, NAPHTHALINUM, PROPYLPARABEN, ANACARDIUM ORIENTALE, GRAPHITES, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), SULPHUR, PARAFFINUM | Energique, Inc. | f3db63df-62a4-48d6-92e7-94e4a5701552 | 2024-12-20 | Warnings | Z8IX2SC1OH A2I8C7HI9T |
| Mirakel Pain and Itch Relief | BENZOCAINE 20%, RESORCINOL 3% | Sanvio, Inc. | ed34d728-0275-e209-e053-2995a90a93ff | 2024-12-20 | Warnings | U3RSY48JW5 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.