Product NDC: | 49825-122 |
Proprietary Name: | Facescreen |
Non Proprietary Name: | Avobenzone, Homosalate, Octinoxate, Octisalate, Octocrylene,Oxybenzone |
Active Ingredient(s): | 3; 10; 7; 5; 5; 6 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; Avobenzone, Homosalate, Octinoxate, Octisalate, Octocrylene,Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49825-122 |
Labeler Name: | Bioelements |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120323 |
Package NDC: | 49825-122-02 |
Package Description: | 1 JAR in 1 CARTON (49825-122-02) > 68 mL in 1 JAR (49825-122-01) (49825-122-01) |
NDC Code | 49825-122-02 |
Proprietary Name | Facescreen |
Package Description | 1 JAR in 1 CARTON (49825-122-02) > 68 mL in 1 JAR (49825-122-01) (49825-122-01) |
Product NDC | 49825-122 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone, Homosalate, Octinoxate, Octisalate, Octocrylene,Oxybenzone |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20120323 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Bioelements |
Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 3; 10; 7; 5; 5; 6 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |