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VIRTUAL SKIN
VIRTUAL SKIN - 59158-759-01 - (OCTINOXATE)
Drug Information of VIRTUAL SKIN
| Product NDC: | 59158-759 |
| Proprietary Name: | VIRTUAL SKIN |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | 5.4 mL/100mL & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of VIRTUAL SKIN
| Product NDC: | 59158-759 |
| Labeler Name: | PRESCRIPTIVES INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19990101 |
Package Information of VIRTUAL SKIN
| Package NDC: | 59158-759-01 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (59158-759-01) > 30 mL in 1 BOTTLE, PLASTIC (59158-759-02) |
NDC Information of VIRTUAL SKIN
| NDC Code | 59158-759-01 |
| Proprietary Name | VIRTUAL SKIN |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (59158-759-01) > 30 mL in 1 BOTTLE, PLASTIC (59158-759-02) |
| Product NDC | 59158-759 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 19990101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | PRESCRIPTIVES INC. |
| Substance Name | OCTINOXATE |
| Strength Number | 5.4 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
