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Peter Island SunscreenSPF 50
Peter Island SunscreenSPF 50 - 10056-702-56 - (HOMOSALATE, OXYBENZONE, OCTISALATE, AVOBENZONE, OCTOCRYLENE)
Drug Information of Peter Island SunscreenSPF 50
| Product NDC: | 10056-702 |
| Proprietary Name: | Peter Island SunscreenSPF 50 |
| Non Proprietary Name: | HOMOSALATE, OXYBENZONE, OCTISALATE, AVOBENZONE, OCTOCRYLENE |
| Active Ingredient(s): | 3; 13; 5; 7; 4 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 SunscreenSPF 50
| Product NDC: | 10056-702 |
| Labeler Name: | Access Business Group LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130627 |
Package Information of Peter Island SunscreenSPF 50
| Package NDC: | 10056-702-56 |
| Package Description: | 226 g in 1 BOTTLE, PLASTIC (10056-702-56) |
NDC Information of Peter Island SunscreenSPF 50
| NDC Code | 10056-702-56 |
| Proprietary Name | Peter Island SunscreenSPF 50 |
| Package Description | 226 g in 1 BOTTLE, PLASTIC (10056-702-56) |
| Product NDC | 10056-702 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HOMOSALATE, OXYBENZONE, OCTISALATE, AVOBENZONE, OCTOCRYLENE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130627 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Access Business Group LLC |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 3; 13; 5; 7; 4 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
