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Premium Whitening
Premium Whitening - 60319-1001-1 - (HYDROGEN PEROXIDE)
Drug Information of Premium Whitening
| Product NDC: | 60319-1001 |
| Proprietary Name: | Premium Whitening |
| Non Proprietary Name: | HYDROGEN PEROXIDE |
| Active Ingredient(s): | 35 mL/100mL & nbsp; HYDROGEN PEROXIDE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | GEL, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Premium Whitening
| Product NDC: | 60319-1001 |
| Labeler Name: | Hankuk Bowonbio Co., Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110913 |
Package Information of Premium Whitening
| Package NDC: | 60319-1001-1 |
| Package Description: | 4.3 mL in 1 BOTTLE, PLASTIC (60319-1001-1) |
NDC Information of Premium Whitening
| NDC Code | 60319-1001-1 |
| Proprietary Name | Premium Whitening |
| Package Description | 4.3 mL in 1 BOTTLE, PLASTIC (60319-1001-1) |
| Product NDC | 60319-1001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HYDROGEN PEROXIDE |
| Dosage Form Name | GEL, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20110913 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Hankuk Bowonbio Co., Ltd |
| Substance Name | HYDROGEN PEROXIDE |
| Strength Number | 35 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
