Home
>
National Drug Code (NDC)
>
Peter Island Ultimate Sheer Dry Touch Sunscreen
Peter Island Ultimate Sheer Dry Touch Sunscreen - 50390-707-12 - (HOMOSALATE, OXYBENZONE, OCTISALATE, AVOBENZONE, OCTOCRYLENE)
Drug Information of Peter Island Ultimate Sheer Dry Touch Sunscreen
| Product NDC: | 50390-707 |
| Proprietary Name: | Peter Island Ultimate Sheer Dry Touch Sunscreen |
| Non Proprietary Name: | HOMOSALATE, OXYBENZONE, OCTISALATE, AVOBENZONE, OCTOCRYLENE |
| Active Ingredient(s): | 3; 15; 5; 2.8; 6 g/100g; g/100g; g/100g; g/100g; g/100g & nbsp; HOMOSALATE, OXYBENZONE, OCTISALATE, AVOBENZONE, OCTOCRYLENE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Peter Island Ultimate Sheer Dry Touch Sunscreen
| Product NDC: | 50390-707 |
| Labeler Name: | AMWAY CORP. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121126 |
Package Information of Peter Island Ultimate Sheer Dry Touch Sunscreen
| Package NDC: | 50390-707-12 |
| Package Description: | 85 g in 1 BOTTLE, PLASTIC (50390-707-12) |
NDC Information of Peter Island Ultimate Sheer Dry Touch Sunscreen
| NDC Code | 50390-707-12 |
| Proprietary Name | Peter Island Ultimate Sheer Dry Touch Sunscreen |
| Package Description | 85 g in 1 BOTTLE, PLASTIC (50390-707-12) |
| Product NDC | 50390-707 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HOMOSALATE, OXYBENZONE, OCTISALATE, AVOBENZONE, OCTOCRYLENE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20121126 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | AMWAY CORP. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 3; 15; 5; 2.8; 6 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
