Point Relief cold Spot Pain Relieving is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by Fabrication Enterprises. The primary component is Menthol.
| Product ID | 51452-038_85799c07-0b9e-20e5-e053-2a91aa0a4f0a |
| NDC | 51452-038 |
| Product Type | Human Otc Drug |
| Proprietary Name | Point Relief cold Spot Pain Relieving |
| Generic Name | Menthol |
| Dosage Form | Spray |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2019-04-01 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part348 |
| Labeler Name | Fabrication Enterprises |
| Substance Name | MENTHOL |
| Active Ingredient Strength | 100 mg/mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2019-04-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph not final |
| Application Number | part348 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-04-01 |
| Marketing Category | OTC monograph not final |
| Application Number | part348 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-04-01 |
| Ingredient | Strength |
|---|---|
| MENTHOL | 100 mg/mL |
| SPL SET ID: | cb593db6-10f3-4276-9f27-e0ccaa9eceb2 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 51452-035 | Point Relief Cold Spot Pain Relieving | Point Relief Cold Spot Pain Relieving |
| 51452-038 | Point Relief cold Spot Pain Relieving | Point Relief cold Spot Pain Relieving |
| 51452-036 | Point Relief Cold Spot Pain Relieving | Point Relief Cold Spot Pain Relieving |
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