| Product NDC: | 44717-536 |
| Proprietary Name: | Tahitian Noni |
| Non Proprietary Name: | Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone |
| Active Ingredient(s): | 2; 6.5; 7; 5; 3 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 44717-536 |
| Labeler Name: | Wasatch Product Development |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100628 |
| Package NDC: | 44717-536-02 |
| Package Description: | 1 BOTTLE in 1 BOX (44717-536-02) > 200 mL in 1 BOTTLE (44717-536-01) |
| NDC Code | 44717-536-02 |
| Proprietary Name | Tahitian Noni |
| Package Description | 1 BOTTLE in 1 BOX (44717-536-02) > 200 mL in 1 BOTTLE (44717-536-01) |
| Product NDC | 44717-536 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100628 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Wasatch Product Development |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 2; 6.5; 7; 5; 3 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |