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Neutrogena Ultra Gentle Soothing
Neutrogena Ultra Gentle Soothing - 10812-531-01 - (Avobenzone, Octinoxate, and Octisalate)
Drug Information of Neutrogena Ultra Gentle Soothing
| Product NDC: | 10812-531 |
| Proprietary Name: | Neutrogena Ultra Gentle Soothing |
| Non Proprietary Name: | Avobenzone, Octinoxate, and Octisalate |
| Active Ingredient(s): | 30; 75; 20 mg/mL; mg/mL; mg/mL & nbsp; Avobenzone, Octinoxate, and Octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Neutrogena Ultra Gentle Soothing
| Product NDC: | 10812-531 |
| Labeler Name: | Neutrogena Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120921 |
Package Information of Neutrogena Ultra Gentle Soothing
| Package NDC: | 10812-531-01 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (10812-531-01) > 118 mL in 1 BOTTLE, PUMP |
NDC Information of Neutrogena Ultra Gentle Soothing
| NDC Code | 10812-531-01 |
| Proprietary Name | Neutrogena Ultra Gentle Soothing |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (10812-531-01) > 118 mL in 1 BOTTLE, PUMP |
| Product NDC | 10812-531 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, and Octisalate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120921 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Neutrogena Corporation |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
| Strength Number | 30; 75; 20 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
