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Neutrogena Blackhead Eliminating Daily Scrub
Neutrogena Blackhead Eliminating Daily Scrub - 10812-129-01 - (Salicylic Acid)
Drug Information of Neutrogena Blackhead Eliminating Daily Scrub
| Product NDC: | 10812-129 |
| Proprietary Name: | Neutrogena Blackhead Eliminating Daily Scrub |
| Non Proprietary Name: | Salicylic Acid |
| Active Ingredient(s): | 20 mg/mL & nbsp; Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Neutrogena Blackhead Eliminating Daily Scrub
| Product NDC: | 10812-129 |
| Labeler Name: | Neutrogena Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120320 |
Package Information of Neutrogena Blackhead Eliminating Daily Scrub
| Package NDC: | 10812-129-01 |
| Package Description: | 125 mL in 1 TUBE (10812-129-01) |
NDC Information of Neutrogena Blackhead Eliminating Daily Scrub
| NDC Code | 10812-129-01 |
| Proprietary Name | Neutrogena Blackhead Eliminating Daily Scrub |
| Package Description | 125 mL in 1 TUBE (10812-129-01) |
| Product NDC | 10812-129 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic Acid |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120320 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Neutrogena Corporation |
| Substance Name | SALICYLIC ACID |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
