Home
>
National Drug Code (NDC)
>
Ambi Essentials
Ambi Essentials - 58232-0504-1 - (Avobenzone, Octisalate, Octocrylene and Oxybenzone)
Drug Information of Ambi Essentials
| Product NDC: | 58232-0504 |
| Proprietary Name: | Ambi Essentials |
| Non Proprietary Name: | Avobenzone, Octisalate, Octocrylene and Oxybenzone |
| Active Ingredient(s): | 30; 50; 17; 30 mg/59mL; mg/59mL; mg/59mL; mg/59mL & nbsp; Avobenzone, Octisalate, Octocrylene and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ambi Essentials
| Product NDC: | 58232-0504 |
| Labeler Name: | Johnson & Johnson Consumer Products Co., Division of Johnson & Johnson Consumer Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100128 |
Package Information of Ambi Essentials
| Package NDC: | 58232-0504-1 |
| Package Description: | 59 mL in 1 TUBE (58232-0504-1) |
NDC Information of Ambi Essentials
| NDC Code | 58232-0504-1 |
| Proprietary Name | Ambi Essentials |
| Package Description | 59 mL in 1 TUBE (58232-0504-1) |
| Product NDC | 58232-0504 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octisalate, Octocrylene and Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100128 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Co., Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | AVOBENZONE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 30; 50; 17; 30 |
| Strength Unit | mg/59mL; mg/59mL; mg/59mL; mg/59mL |
| Pharmaceutical Classes |
