| Product NDC: | 16555-006 |
| Proprietary Name: | VIALPROTECTION |
| Non Proprietary Name: | HOMOSALATE, OCTISALATE, AVOBENZONE OXYBENZONE |
| Active Ingredient(s): | 3; 5; 5; 3 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; HOMOSALATE, OCTISALATE, AVOBENZONE OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 16555-006 |
| Labeler Name: | DARPHIN DIST. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090901 |
| Package NDC: | 16555-006-01 |
| Package Description: | 1 TUBE in 1 CARTON (16555-006-01) > 50 mL in 1 TUBE (16555-006-02) |
| NDC Code | 16555-006-01 |
| Proprietary Name | VIALPROTECTION |
| Package Description | 1 TUBE in 1 CARTON (16555-006-01) > 50 mL in 1 TUBE (16555-006-02) |
| Product NDC | 16555-006 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HOMOSALATE, OCTISALATE, AVOBENZONE OXYBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | DARPHIN DIST. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OXYBENZONE |
| Strength Number | 3; 5; 5; 3 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |