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NO-AD 15 Sunscreen
NO-AD 15 Sunscreen - 62802-212-16 - (avobenzone, homosalate,octisalate)
Drug Information of NO-AD 15 Sunscreen
| Product NDC: | 62802-212 |
| Proprietary Name: | NO-AD 15 Sunscreen |
| Non Proprietary Name: | avobenzone, homosalate,octisalate |
| Active Ingredient(s): | 1.2; 7.5; 5 mL/100mL; mL/100mL; mL/100mL & nbsp; avobenzone, homosalate,octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NO-AD 15 Sunscreen
| Product NDC: | 62802-212 |
| Labeler Name: | Sun & Skin Care Research, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120101 |
Package Information of NO-AD 15 Sunscreen
| Package NDC: | 62802-212-16 |
| Package Description: | 475 mL in 1 BOTTLE (62802-212-16) |
NDC Information of NO-AD 15 Sunscreen
| NDC Code | 62802-212-16 |
| Proprietary Name | NO-AD 15 Sunscreen |
| Package Description | 475 mL in 1 BOTTLE (62802-212-16) |
| Product NDC | 62802-212 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | avobenzone, homosalate,octisalate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Sun & Skin Care Research, LLC |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE |
| Strength Number | 1.2; 7.5; 5 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
