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Aqualant
Aqualant - 52205-002-00 - (DIMETHICONE)
Drug Information of Aqualant
| Product NDC: | 52205-002 |
| Proprietary Name: | Aqualant |
| Non Proprietary Name: | DIMETHICONE |
| Active Ingredient(s): | 24.92 mL/100mL & nbsp; DIMETHICONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OIL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aqualant
| Product NDC: | 52205-002 |
| Labeler Name: | Advanced Skin Technology, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120904 |
Package Information of Aqualant
| Package NDC: | 52205-002-00 |
| Package Description: | 177 mL in 1 BOTTLE (52205-002-00) |
NDC Information of Aqualant
| NDC Code | 52205-002-00 |
| Proprietary Name | Aqualant |
| Package Description | 177 mL in 1 BOTTLE (52205-002-00) |
| Product NDC | 52205-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIMETHICONE |
| Dosage Form Name | OIL |
| Route Name | TOPICAL |
| Start Marketing Date | 20120904 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Advanced Skin Technology, LLC |
| Substance Name | DIMETHICONE |
| Strength Number | 24.92 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
