| 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 |