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NO-AD Splash 30 Sunscreen
NO-AD Splash 30 Sunscreen - 62802-213-16 - (avobenzone, homosalate, octisalate, oxybenzone)
Drug Information of NO-AD Splash 30 Sunscreen
| Product NDC: | 62802-213 |
| Proprietary Name: | NO-AD Splash 30 Sunscreen |
| Non Proprietary Name: | avobenzone, homosalate, octisalate, oxybenzone |
| Active Ingredient(s): | 2; 10; 5; 3 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; avobenzone, homosalate, octisalate, oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NO-AD Splash 30 Sunscreen
| Product NDC: | 62802-213 |
| 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 Splash 30 Sunscreen
| Package NDC: | 62802-213-16 |
| Package Description: | 475 mL in 1 BOTTLE (62802-213-16) |
NDC Information of NO-AD Splash 30 Sunscreen
| NDC Code | 62802-213-16 |
| Proprietary Name | NO-AD Splash 30 Sunscreen |
| Package Description | 475 mL in 1 BOTTLE (62802-213-16) |
| Product NDC | 62802-213 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | avobenzone, homosalate, octisalate, oxybenzone |
| 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; OXYBENZONE |
| Strength Number | 2; 10; 5; 3 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
