GOLD ICE Pain Relief
- Product NDC
- 72226-305
- 11-digit product format
- 722260305
- Labeler code
- 72226
- Product ID
- 72226-305_09dc4870-a264-48af-e063-6394a90aa79e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Eden's Answers, Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-08-01
- Substance
- MENTHOL
- Active strength
- 62.5 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- GOLD ICE Pain Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 62.5 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 2003750 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72226-305-00 | GOLD ICE Pain Relief | 1 in 1 BOX | CREAM | 1 | | 2 |
| 72226-305-00 | GOLD ICE Pain Relief | 100 mL in 1 TUBE | CREAM | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72226-305 | GOLD ICE PAIN RELIEF (MENTHOL) CREAM [EDEN'S ANSWERS, INC.] | 2 | Current NDC, Legacy NDC, 2 package rows | 20231112_a1356c39-42b9-4bd8-a873-bcd40717058b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72226-305-00 | 72226030500 | 1 TUBE in 1 BOX (72226-305-00) / 100 mL in 1 TUBE | 1 tube | 2020-08-01 | 0000-00-00 | No | No | Current |