Product NDC: | 49825-120 |
Proprietary Name: | Sun Diffusing Protector |
Non Proprietary Name: | Avobenzone, Homosalate, Octocrylene, Octyl Salicylate, Oxybenzone |
Active Ingredient(s): | 2; 7.5; 5; 1.8; .49 mL/100mL; mL/100mL; mm/100mL; mL/100mL; mL/100mL & nbsp; Avobenzone, Homosalate, Octocrylene, Octyl Salicylate, Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49825-120 |
Labeler Name: | Bioelements Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120321 |
Package NDC: | 49825-120-02 |
Package Description: | 1 TUBE in 1 CARTON (49825-120-02) > 118 mL in 1 TUBE (49825-120-01) (49825-120-01) |
NDC Code | 49825-120-02 |
Proprietary Name | Sun Diffusing Protector |
Package Description | 1 TUBE in 1 CARTON (49825-120-02) > 118 mL in 1 TUBE (49825-120-01) (49825-120-01) |
Product NDC | 49825-120 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone, Homosalate, Octocrylene, Octyl Salicylate, Oxybenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120321 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Bioelements Inc |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 2; 7.5; 5; 1.8; .49 |
Strength Unit | mL/100mL; mL/100mL; mm/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |