NDC 74146-239-01 - Instant Gel
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
- 74146-239
- Requested NDC
- 74146-239-01
- Package NDCs from labels
- 74146-239-01, 74146-239-10, 74146-239-02, 74146-239-11, 74146-239-03, 74146-239-12, 74146-239-04, 74146-239-13, 74146-239-05, 74146-239-14, 74146-239-06, 74146-239-15, 74146-239-07, 74146-239-16
- Manufacturer
- GM Industrial, Inc.
- Effective date
- 2020-12-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Instant Gel - GM Industrial, Inc. | GM Industrial, Inc. | 2020-12-10 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 74146-239-01 | Instant Gel | 3785.41 mL in 1 CONTAINER | GEL | 3785.41 | 4 | |
| 74146-239-02 | Instant Gel | 1000 mL in 1 JUG | GEL | 1000 | 4 | |
| 74146-239-03 | Instant Gel | 2500 mL in 1 JUG | GEL | 2500 | 4 | |
| 74146-239-04 | Instant Gel | 3550 mL in 1 JUG | GEL | 3550 | 4 | |
| 74146-239-05 | Instant Gel | 100 mL in 1 CONTAINER | GEL | 100 | 4 | |
| 74146-239-06 | Instant Gel | 200 mL in 1 CONTAINER | GEL | 200 | 4 | |
| 74146-239-07 | Instant Gel | 946.35 mL in 1 CONTAINER | GEL | 946.35 | 4 | |
| 74146-239-10 | Instant Gel | 4 in 1 BOX | GEL | 4 | 4 | |
| 74146-239-11 | Instant Gel | 4 in 1 BOX | GEL | 4 | 4 | |
| 74146-239-12 | Instant Gel | 4 in 1 BOX | GEL | 4 | 4 | |
| 74146-239-13 | Instant Gel | 4 in 1 BOX | GEL | 4 | 4 | |
| 74146-239-14 | Instant Gel | 96 in 1 BOX | GEL | 96 | 4 | |
| 74146-239-15 | Instant Gel | 24 in 1 BOX | GEL | 24 | 4 | |
| 74146-239-16 | Instant Gel | 12 in 1 BOX | GEL | 12 | 4 |
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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| Antiseptic Wipes | ANTISEPTIC WIPES | Front Line Safety | 0e1f3653-d75e-9c9e-e063-6294a90ab639 | 2025-12-15 | Warnings | F5UM2KM3W7 |
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| First Aid Burn Cream | FIRST AID BURN CREAM | Front Line Safety | 0f4ce2c2-f306-d95f-e063-6394a90ae7b3 | 2025-12-15 | Warnings | F5UM2KM3W7 |
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| Dial Antibacterial Vitamin Bar | DIAL ANTIBACTERIAL VITAMIN BAR SOAP | Henkel Corporation | 292bf620-5cde-388d-e063-6394a90a307c | 2025-12-11 | Warnings | F5UM2KM3W7 |
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| Bright Amber Antibacterial | BENZALKONIUM CHLORIDE | Colgate-Palmolive Company | 44f9cf18-dd2d-4637-a5e1-3db82a1904ff | 2025-12-11 | Warnings | F5UM2KM3W7 |
| HurriCaine One | TOPICAL ANESTHETIC AND ANTISEPTIC | Beutlich Pharmaceuticals LLC | 459cedbd-9b6f-e450-e063-6394a90afb73 | 2025-12-10 | Warnings | F5UM2KM3W7 |
| Dial Professional Antibacterial Defense Spring Water | BENZALKONIUM CHLORIDE | Henkel Corporation | 29644a9d-3954-a6e5-e063-6394a90a82c7 | 2025-12-09 | Warnings | F5UM2KM3W7 |
| Dial Professional Antibacterial Foaming Hand Wash Spring Water | DIAL PROFESSIONAL ANTIBACTERIAL FOAMING HAND SOAP SPRING WATER SCENT | Henkel Corporation | 28dc867c-ca9b-4631-e063-6394a90a9a35 | 2025-12-09 | Warnings | F5UM2KM3W7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.