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skin effects Brightening Day SPF 50
skin effects Brightening Day SPF 50 - 42877-002-01 - (AVOBENZONE, HOMOSALATE, OCTINOXATE,OCTISALATE)
Drug Information of skin effects Brightening Day SPF 50
| Product NDC: | 42877-002 |
| Proprietary Name: | skin effects Brightening Day SPF 50 |
| Non Proprietary Name: | AVOBENZONE, HOMOSALATE, OCTINOXATE,OCTISALATE |
| Active Ingredient(s): | 3; 15; 7.5; 5 g/100g; g/100g; g/100g; g/100g & nbsp; AVOBENZONE, HOMOSALATE, OCTINOXATE,OCTISALATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of skin effects Brightening Day SPF 50
| Product NDC: | 42877-002 |
| Labeler Name: | Diversified Global Technologies DBA Diversified Distribution |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110928 |
Package Information of skin effects Brightening Day SPF 50
| Package NDC: | 42877-002-01 |
| Package Description: | 28.3 g in 1 BOTTLE (42877-002-01) |
NDC Information of skin effects Brightening Day SPF 50
| NDC Code | 42877-002-01 |
| Proprietary Name | skin effects Brightening Day SPF 50 |
| Package Description | 28.3 g in 1 BOTTLE (42877-002-01) |
| Product NDC | 42877-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, HOMOSALATE, OCTINOXATE,OCTISALATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110928 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Diversified Global Technologies DBA Diversified Distribution |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE |
| Strength Number | 3; 15; 7.5; 5 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
