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shing-Releev
shing-Releev - 15478-005-02 - (Benzalkonium Chloride)
Drug Information of shing-Releev
| Product NDC: | 15478-005 |
| Proprietary Name: | shing-Releev |
| Non Proprietary Name: | Benzalkonium Chloride |
| Active Ingredient(s): | 5; 1.3; 5 mL/mL; mL/mL; mL/mL & nbsp; Benzalkonium Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of shing-Releev
| Product NDC: | 15478-005 |
| Labeler Name: | Topical Pharmaceuticals Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100714 |
Package Information of shing-Releev
| Package NDC: | 15478-005-02 |
| Package Description: | 1 BOTTLE, SPRAY in 1 BOX (15478-005-02) > 60 mL in 1 BOTTLE, SPRAY (15478-005-01) |
NDC Information of shing-Releev
| NDC Code | 15478-005-02 |
| Proprietary Name | shing-Releev |
| Package Description | 1 BOTTLE, SPRAY in 1 BOX (15478-005-02) > 60 mL in 1 BOTTLE, SPRAY (15478-005-01) |
| Product NDC | 15478-005 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100714 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Topical Pharmaceuticals Inc. |
| Substance Name | ALLANTOIN; BENZALKONIUM CHLORIDE; BENZYL ALCOHOL |
| Strength Number | 5; 1.3; 5 |
| Strength Unit | mL/mL; mL/mL; mL/mL |
| Pharmaceutical Classes |
