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DERMATOLOGICAL SUN PROTECTION
DERMATOLOGICAL SUN PROTECTION - 76450-051-01 - (OCTINOXATE)
Drug Information of DERMATOLOGICAL SUN PROTECTION
| Product NDC: | 76450-051 |
| Proprietary Name: | DERMATOLOGICAL SUN PROTECTION |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | 1.75; 1.5; 3.75; 3; 2; 3.5 mL/50mL; mL/50mL; mL/50mL; mL/50mL; mL/50mL; mL/50mL & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DERMATOLOGICAL SUN PROTECTION
| Product NDC: | 76450-051 |
| Labeler Name: | Mesoestetic, S.L. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120201 |
Package Information of DERMATOLOGICAL SUN PROTECTION
| Package NDC: | 76450-051-01 |
| Package Description: | 50 mL in 1 TUBE (76450-051-01) |
NDC Information of DERMATOLOGICAL SUN PROTECTION
| NDC Code | 76450-051-01 |
| Proprietary Name | DERMATOLOGICAL SUN PROTECTION |
| Package Description | 50 mL in 1 TUBE (76450-051-01) |
| Product NDC | 76450-051 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Mesoestetic, S.L. |
| Substance Name | AVOBENZONE; ENSULIZOLE; OCTINOXATE; OCTOCRYLENE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 1.75; 1.5; 3.75; 3; 2; 3.5 |
| Strength Unit | mL/50mL; mL/50mL; mL/50mL; mL/50mL; mL/50mL; mL/50mL |
| Pharmaceutical Classes |
