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MINERALIZE
MINERALIZE - 40046-0042-1 - (OCTINOXATE)
Drug Information of MINERALIZE
| Product NDC: | 40046-0042 |
| Proprietary Name: | MINERALIZE |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | 7.5 mL/100mL & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MINERALIZE
| Product NDC: | 40046-0042 |
| Labeler Name: | MAKEUP ART COSMETICS |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20060901 |
Package Information of MINERALIZE
| Package NDC: | 40046-0042-1 |
| Package Description: | 1 BOTTLE, GLASS in 1 CARTON (40046-0042-1) > 30 mL in 1 BOTTLE, GLASS (40046-0042-2) |
NDC Information of MINERALIZE
| NDC Code | 40046-0042-1 |
| Proprietary Name | MINERALIZE |
| Package Description | 1 BOTTLE, GLASS in 1 CARTON (40046-0042-1) > 30 mL in 1 BOTTLE, GLASS (40046-0042-2) |
| Product NDC | 40046-0042 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20060901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | MAKEUP ART COSMETICS |
| Substance Name | OCTINOXATE |
| Strength Number | 7.5 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
