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SUN PREMIUM FACE 50 SPF
SUN PREMIUM FACE 50 SPF - 75870-006-02 - (OXYBENZONE, OCTINOXATE, AVOBENZONE, TITANIUM DIOXIDE)
Drug Information of SUN PREMIUM FACE 50 SPF
| Product NDC: | 75870-006 |
| Proprietary Name: | SUN PREMIUM FACE 50 SPF |
| Non Proprietary Name: | OXYBENZONE, OCTINOXATE, AVOBENZONE, TITANIUM DIOXIDE |
| Active Ingredient(s): | 1.5; 3.75; 3.75; 1.185 mL/75mL; mL/75mL; mL/75mL; mL/75mL & nbsp; OXYBENZONE, OCTINOXATE, AVOBENZONE, TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUN PREMIUM FACE 50 SPF
| Product NDC: | 75870-006 |
| Labeler Name: | LABORATORIOS DE COSMETICA SCIENTIFICA ATACHE SA |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20070515 |
Package Information of SUN PREMIUM FACE 50 SPF
| Package NDC: | 75870-006-02 |
| Package Description: | 1 TUBE in 1 CARTON (75870-006-02) > 75 mL in 1 TUBE (75870-006-01) |
NDC Information of SUN PREMIUM FACE 50 SPF
| NDC Code | 75870-006-02 |
| Proprietary Name | SUN PREMIUM FACE 50 SPF |
| Package Description | 1 TUBE in 1 CARTON (75870-006-02) > 75 mL in 1 TUBE (75870-006-01) |
| Product NDC | 75870-006 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OXYBENZONE, OCTINOXATE, AVOBENZONE, TITANIUM DIOXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20070515 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | LABORATORIOS DE COSMETICA SCIENTIFICA ATACHE SA |
| Substance Name | AVOBENZONE; OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 1.5; 3.75; 3.75; 1.185 |
| Strength Unit | mL/75mL; mL/75mL; mL/75mL; mL/75mL |
| Pharmaceutical Classes |
