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CX DAILY EYE PROTECTOR
CX DAILY EYE PROTECTOR - 49527-750-01 - (TITANIUM DIOXIDE)
Drug Information of CX DAILY EYE PROTECTOR
| Product NDC: | 49527-750 |
| Proprietary Name: | CX DAILY EYE PROTECTOR |
| Non Proprietary Name: | TITANIUM DIOXIDE |
| Active Ingredient(s): | 7.8 mL/100mL & nbsp; TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CX DAILY EYE PROTECTOR
| Product NDC: | 49527-750 |
| Labeler Name: | CLINIQUE LABORATORIES INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20020201 |
Package Information of CX DAILY EYE PROTECTOR
| Package NDC: | 49527-750-01 |
| Package Description: | 1 TUBE in 1 CARTON (49527-750-01) > 7 mL in 1 TUBE (49527-750-02) |
NDC Information of CX DAILY EYE PROTECTOR
| NDC Code | 49527-750-01 |
| Proprietary Name | CX DAILY EYE PROTECTOR |
| Package Description | 1 TUBE in 1 CARTON (49527-750-01) > 7 mL in 1 TUBE (49527-750-02) |
| Product NDC | 49527-750 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20020201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CLINIQUE LABORATORIES INC |
| Substance Name | TITANIUM DIOXIDE |
| Strength Number | 7.8 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
