ZO MEDICAL SURFATROL Astringent is a Topical Powder in the Human Otc Drug category. It is labeled and distributed by Zo Skin Health, Inc.. The primary component is Aluminum Acetate.
| Product ID | 42851-084_af2e1f39-b312-41f4-923c-18a4dff99e1f |
| NDC | 42851-084 |
| Product Type | Human Otc Drug |
| Proprietary Name | ZO MEDICAL SURFATROL Astringent |
| Generic Name | Aluminum Acetate |
| Dosage Form | Powder |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2016-08-01 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part347 |
| Labeler Name | ZO Skin Health, Inc. |
| Substance Name | ALUMINUM ACETATE |
| Active Ingredient Strength | 4866 mg/4.866g |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 2016-08-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-08-01 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| ALUMINUM ACETATE | 4866 mg/4.866g |
| SPL SET ID: | 82f31fa8-960f-42c4-a0b1-9f91bad825b3 |
| Manufacturer | |
| UNII |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 42851-084 | ZO MEDICAL SURFATROL Astringent | Aluminum Acetate |
| 35192-005 | Astringent | Aluminum Acetate |
| 81507-001 | Dermaleve | Aluminum Acetate |
| 81507-002 | Dermeleve | Aluminum Acetate |
| 81507-003 | Dermeleve | Aluminum Acetate |
| 16864-250 | DOMEBORO | Aluminum Acetate |
| 16864-192 | Domeboro Cooling | Aluminum Acetate |
| 71207-100 | TriCalm | Aluminum Acetate |
| 76312-001 | TriCalm | Aluminum Acetate |
| 76312-002 | TriCalm | Aluminum Acetate |
| 42851-090 | ZO Skin Health Astringent Solution | Aluminum Acetate |
| 42851-187 | ZO Skin Health Post Procedure Program | ALUMINUM ACETATE |
| 42851-193 | ZO Skin Health Post Procedure Recovery System | Aluminum Acetate |