EXTRA STRENGTH eez-away is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Eezaway Relief Inc. The primary component is Menthol, Unspec.
Product ID | 69678-121_1a157eb6-8e54-4e90-89a2-4b1e0fa5cef6 |
NDC | 69678-121 |
Product Type | Human Otc Drug |
Proprietary Name | EXTRA STRENGTH eez-away |
Generic Name | Menthol |
Dosage Form | Liquid |
Route of Administration | TOPICAL |
Marketing Start Date | 2019-03-13 |
Marketing Category | OTC MONOGRAPH N / OTC MONOGRAPH NOT FINAL |
Application Number | part348 |
Labeler Name | EEZAWAY RELIEF INC |
Substance Name | MENTHOL, UNSPEC |
Active Ingredient Strength | 3 g/100mL |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2019-03-13 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph not final |
Application Number | part348 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2019-03-13 |
Ingredient | Strength |
---|---|
MENTHOL, UNSPECIFIED FORM | 2.5 g/100mL |
SPL SET ID: | b2790dd6-6eac-4106-9a98-7bd600edec9a |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
69678-121 | EXTRA STRENGTH eez-away | EXTRA STRENGTH eez-away |
69678-131 | EXTRA STRENGTH eez-away | EXTRA STRENGTH eez-away |
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