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NDC 11673-0510-10 Maximum Strength Medicated Foot Powder 0.1 g/g Details
Maximum Strength Medicated Foot Powder 0.1 g/g
Maximum Strength Medicated Foot Powder is a TOPICAL POWDER in the HUMAN OTC DRUG category. It is labeled and distributed by Target Corporation. The primary component is MENTHOL.
Product Information
| NDC | 11673-0510 |
|---|---|
| Product ID | 11673-510_f37fea91-1dcd-5fef-e053-2a95a90a3fc6 |
| Associated GPIs | |
| GCN Sequence Number | 043020 |
| GCN Sequence Number Description | menthol POWDER 1 % TOPICAL |
| HIC3 | L6A |
| HIC3 Description | IRRITANTS/COUNTER-IRRITANTS |
| GCN | 23821 |
| HICL Sequence Number | 002608 |
| HICL Sequence Number Description | MENTHOL |
| Brand/Generic | Generic |
| Proprietary Name | Maximum Strength Medicated Foot Powder |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Medicated Foot Powder |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | POWDER |
| Route | TOPICAL |
| Active Ingredient Strength | 0.1 |
| Active Ingredient Units | g/g |
| Substance Name | MENTHOL |
| Labeler Name | Target Corporation |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part348 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 11673-0510-10 (11673051010)
| NDC Package Code | 11673-510-10 |
|---|---|
| Billing NDC | 11673051010 |
| Package | 283 g in 1 BOTTLE, PLASTIC (11673-510-10) |
| Marketing Start Date | 2013-04-30 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |