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OP Protective Spray Gel 8
OP Protective Spray Gel 8 - 62802-038-85 - (octinoxate, octisalate)
Drug Information of OP Protective Spray Gel 8
| Product NDC: | 62802-038 |
| Proprietary Name: | OP Protective Spray Gel 8 |
| Non Proprietary Name: | octinoxate, octisalate |
| Active Ingredient(s): | 4.5; 5 mL/100mL; mL/100mL & nbsp; octinoxate, octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OP Protective Spray Gel 8
| Product NDC: | 62802-038 |
| Labeler Name: | Sun & Skin Care Research, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120101 |
Package Information of OP Protective Spray Gel 8
| Package NDC: | 62802-038-85 |
| Package Description: | 251 mL in 1 BOTTLE (62802-038-85) |
NDC Information of OP Protective Spray Gel 8
| NDC Code | 62802-038-85 |
| Proprietary Name | OP Protective Spray Gel 8 |
| Package Description | 251 mL in 1 BOTTLE (62802-038-85) |
| Product NDC | 62802-038 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | octinoxate, octisalate |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20120101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Sun & Skin Care Research, Inc |
| Substance Name | OCTINOXATE; OCTISALATE |
| Strength Number | 4.5; 5 |
| Strength Unit | mL/100mL; mL/100mL |
| Pharmaceutical Classes |
