Product NDC: | 64942-1244 |
Proprietary Name: | Simple |
Non Proprietary Name: | Homosalate, Octisalate, Avobenzone, and Octocrylene |
Active Ingredient(s): | .03; .12; .05; .027 g/g; g/g; g/g; g/g & nbsp; Homosalate, Octisalate, Avobenzone, and Octocrylene |
Administration Route(s): | TOPICAL |
Dosage Form(s): | EMULSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64942-1244 |
Labeler Name: | CONOPCO Inc. d/b/a Unilever |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120301 |
Package NDC: | 64942-1244-2 |
Package Description: | 1 JAR in 1 CARTON (64942-1244-2) > 50 g in 1 JAR (64942-1244-1) |
NDC Code | 64942-1244-2 |
Proprietary Name | Simple |
Package Description | 1 JAR in 1 CARTON (64942-1244-2) > 50 g in 1 JAR (64942-1244-1) |
Product NDC | 64942-1244 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Homosalate, Octisalate, Avobenzone, and Octocrylene |
Dosage Form Name | EMULSION |
Route Name | TOPICAL |
Start Marketing Date | 20120301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CONOPCO Inc. d/b/a Unilever |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
Strength Number | .03; .12; .05; .027 |
Strength Unit | g/g; g/g; g/g; g/g |
Pharmaceutical Classes |