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SODIUM HYDROXIDE
SODIUM HYDROXIDE - 10481-3006-1 - (SODIUM HYDROXIDE)
Drug Information of SODIUM HYDROXIDE
| Product NDC: | 10481-3006 |
| Proprietary Name: | SODIUM HYDROXIDE |
| Non Proprietary Name: | SODIUM HYDROXIDE |
| Active Ingredient(s): | .01 g/g & nbsp; SODIUM HYDROXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SODIUM HYDROXIDE
| Product NDC: | 10481-3006 |
| Labeler Name: | Gordon Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100716 |
Package Information of SODIUM HYDROXIDE
| Package NDC: | 10481-3006-1 |
| Package Description: | 59 g in 1 BOTTLE, GLASS (10481-3006-1) |
NDC Information of SODIUM HYDROXIDE
| NDC Code | 10481-3006-1 |
| Proprietary Name | SODIUM HYDROXIDE |
| Package Description | 59 g in 1 BOTTLE, GLASS (10481-3006-1) |
| Product NDC | 10481-3006 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM HYDROXIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100716 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Gordon Laboratories |
| Substance Name | SODIUM HYDROXIDE |
| Strength Number | .01 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
