Natralia Cramp Relief is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Laderma Trading Pty Ltd. The primary component is Methyl Salicylate.
| Product ID | 43251-3213_b76aa734-54d8-4a3f-aefd-963d68b1051c |
| NDC | 43251-3213 |
| Product Type | Human Otc Drug |
| Proprietary Name | Natralia Cramp Relief |
| Generic Name | Methyl Salicylate |
| Dosage Form | Gel |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2009-03-01 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | Laderma Trading Pty Ltd |
| Substance Name | METHYL SALICYLATE |
| Active Ingredient Strength | 105 mg/g |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2009-03-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2009-03-01 |
| Inactivation Date | 2019-10-29 |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2009-03-01 |
| Inactivation Date | 2019-10-29 |
| Ingredient | Strength |
|---|---|
| METHYL SALICYLATE | 105 mg/g |
| SPL SET ID: | d6c85b92-08bc-45de-9cec-43e49c707670 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 43251-3213 | Natralia Cramp Relief | Methyl Salicylate |
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| 33346-3401 | Mobility | Methyl salicylate |
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