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 |