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Radiant C UVA/UVB Sunscreen
Radiant C UVA/UVB Sunscreen - 51785-445-01 - (Avobenzone, Octinoxate, and Oxybenzone)
Drug Information of Radiant C UVA/UVB Sunscreen
| Product NDC: | 51785-445 |
| Proprietary Name: | Radiant C UVA/UVB Sunscreen |
| Non Proprietary Name: | Avobenzone, Octinoxate, and Oxybenzone |
| Active Ingredient(s): | .03; .07; .004 g/mL; g/mL; g/mL & nbsp; Avobenzone, Octinoxate, and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Radiant C UVA/UVB Sunscreen
| Product NDC: | 51785-445 |
| Labeler Name: | Herbalife International of America |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130401 |
Package Information of Radiant C UVA/UVB Sunscreen
| Package NDC: | 51785-445-01 |
| Package Description: | 200 mL in 1 TUBE (51785-445-01) |
NDC Information of Radiant C UVA/UVB Sunscreen
| NDC Code | 51785-445-01 |
| Proprietary Name | Radiant C UVA/UVB Sunscreen |
| Package Description | 200 mL in 1 TUBE (51785-445-01) |
| Product NDC | 51785-445 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, and Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130401 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Herbalife International of America |
| Substance Name | AVOBENZONE; OCTINOXATE; OXYBENZONE |
| Strength Number | .03; .07; .004 |
| Strength Unit | g/mL; g/mL; g/mL |
| Pharmaceutical Classes |
