Product NDC: | 54473-122 |
Proprietary Name: | SunShades |
Non Proprietary Name: | Octinoxate and Oxybenzone |
Active Ingredient(s): | 75; 30 mg/g; mg/g & nbsp; Octinoxate and Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | STICK |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54473-122 |
Labeler Name: | Melaleuca, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20070801 |
Package NDC: | 54473-122-04 |
Package Description: | 4.2 g in 1 APPLICATOR (54473-122-04) |
NDC Code | 54473-122-04 |
Proprietary Name | SunShades |
Package Description | 4.2 g in 1 APPLICATOR (54473-122-04) |
Product NDC | 54473-122 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate and Oxybenzone |
Dosage Form Name | STICK |
Route Name | TOPICAL |
Start Marketing Date | 20070801 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Melaleuca, Inc. |
Substance Name | OCTINOXATE; OXYBENZONE |
Strength Number | 75; 30 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes |