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Solutions - 10096-0168-3 - (OCTINOXATE, OCTISALATE, AVOBENZONE)
Drug Information of Solutions
| Product NDC: | 10096-0168 |
| Proprietary Name: | Solutions |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, AVOBENZONE |
| Active Ingredient(s): | 20; 75; 50 mg/mL; mg/mL; mg/mL & nbsp; OCTINOXATE, OCTISALATE, AVOBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Solutions
| Product NDC: | 10096-0168 |
| Labeler Name: | Avon Products, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130208 |
Package Information of Solutions
| Package NDC: | 10096-0168-3 |
| Package Description: | 1.1 mL in 1 PACKAGE (10096-0168-3) |
NDC Information of Solutions
| NDC Code | 10096-0168-3 |
| Proprietary Name | Solutions |
| Package Description | 1.1 mL in 1 PACKAGE (10096-0168-3) |
| Product NDC | 10096-0168 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, AVOBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130208 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Avon Products, Inc |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
| Strength Number | 20; 75; 50 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
