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Arbonne Revelage
Arbonne Revelage - 42508-137-32 - (HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, and OXYBENZONE)
Drug Information of Arbonne Revelage
| Product NDC: | 42508-137 |
| Proprietary Name: | Arbonne Revelage |
| Non Proprietary Name: | HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, and OXYBENZONE |
| Active Ingredient(s): | 80; 75; 50; 30; 30 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp; HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, and OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Arbonne Revelage
| Product NDC: | 42508-137 |
| Labeler Name: | Arbonne International, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100803 |
Package Information of Arbonne Revelage
| Package NDC: | 42508-137-32 |
| Package Description: | 1 TUBE in 1 CARTON (42508-137-32) > 74 mL in 1 TUBE |
NDC Information of Arbonne Revelage
| NDC Code | 42508-137-32 |
| Proprietary Name | Arbonne Revelage |
| Package Description | 1 TUBE in 1 CARTON (42508-137-32) > 74 mL in 1 TUBE |
| Product NDC | 42508-137 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, and OXYBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100803 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Arbonne International, LLC |
| Substance Name | HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 80; 75; 50; 30; 30 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
