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 |