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NU SKIN
NU SKIN - 62839-0289-1 - (Avobenzone, Homosalate, Octisalate, and Octocrylene)
Drug Information of NU SKIN
| Product NDC: | 62839-0289 |
| Proprietary Name: | NU SKIN |
| Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Active Ingredient(s): | 3; 5; 4; 2 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NU SKIN
| Product NDC: | 62839-0289 |
| Labeler Name: | NSE Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20091001 |
Package Information of NU SKIN
| Package NDC: | 62839-0289-1 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (62839-0289-1) > 15 mL in 1 BOTTLE, PUMP |
NDC Information of NU SKIN
| NDC Code | 62839-0289-1 |
| Proprietary Name | NU SKIN |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (62839-0289-1) > 15 mL in 1 BOTTLE, PUMP |
| Product NDC | 62839-0289 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20091001 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | NSE Products, Inc. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 3; 5; 4; 2 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
