Product NDC: | 58232-0606 |
Proprietary Name: | Ambi Even and Clear Daily Moisturizer |
Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone |
Active Ingredient(s): | 30; 120; 50; 17; 30 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 58232-0606 |
Labeler Name: | Johnson & Johnson Consumer Products Company, 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: | 20120724 |
Package NDC: | 58232-0606-1 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (58232-0606-1) > 88 mL in 1 BOTTLE, PLASTIC |
NDC Code | 58232-0606-1 |
Proprietary Name | Ambi Even and Clear Daily Moisturizer |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (58232-0606-1) > 88 mL in 1 BOTTLE, PLASTIC |
Product NDC | 58232-0606 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120724 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 30; 120; 50; 17; 30 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |