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ORIGINAL POWER WHITENING AND LINELESS AMPOULE
ORIGINAL POWER WHITENING AND LINELESS AMPOULE - 51346-219-01 - (ALLANTOIN)
Drug Information of ORIGINAL POWER WHITENING AND LINELESS AMPOULE
| Product NDC: | 51346-219 |
| Proprietary Name: | ORIGINAL POWER WHITENING AND LINELESS AMPOULE |
| Non Proprietary Name: | ALLANTOIN |
| Active Ingredient(s): | .54 mg/30mL & nbsp; ALLANTOIN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ORIGINAL POWER WHITENING AND LINELESS AMPOULE
| Product NDC: | 51346-219 |
| Labeler Name: | NATURE REPUBLIC CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130201 |
Package Information of ORIGINAL POWER WHITENING AND LINELESS AMPOULE
| Package NDC: | 51346-219-01 |
| Package Description: | 30 mL in 1 CARTON (51346-219-01) |
NDC Information of ORIGINAL POWER WHITENING AND LINELESS AMPOULE
| NDC Code | 51346-219-01 |
| Proprietary Name | ORIGINAL POWER WHITENING AND LINELESS AMPOULE |
| Package Description | 30 mL in 1 CARTON (51346-219-01) |
| Product NDC | 51346-219 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALLANTOIN |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | NATURE REPUBLIC CO., LTD. |
| Substance Name | ALLANTOIN |
| Strength Number | .54 |
| Strength Unit | mg/30mL |
| Pharmaceutical Classes |
