Tommie Copper Foot
- Product NDC
- 72562-222
- 11-digit product format
- 725620222
- Labeler code
- 72562
- Product ID
- 72562-222_2959377c-1b3c-64f8-e063-6394a90aaeae
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dimethicone 1%
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Tommie Copper, Inc.
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-08-19
- Substance
- DIMETHICONE
- Active strength
- 1 g/100g
- Pharmacologic classes
- Skin Barrier Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tommie Copper Foot
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIMETHICONE | 1 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 92RU3N3Y1O |
| Rxcui | 200010 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72562-222-01 | Tommie Copper Foot | 28 g in 1 TUBE | CREAM | 28 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72562-222 | TOMMIE COPPER FOOT (DIMETHICONE 1%) CREAM [TOMMIE COPPER, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20241217_ca3d3374-a3d4-69e5-e053-2995a90a3ece.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 |
|---|
| 72562-222-01 | 72562022201 | 28 g in 1 TUBE (72562-222-01) | 28 g | 2021-08-19 | 0000-00-00 | No | No | Current |