| Product NDC: | 54473-161 |
| Proprietary Name: | SUN SHADES |
| 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: | 54473-161 |
| Labeler Name: | Melaleuca, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20081001 |
| Package NDC: | 54473-161-01 |
| Package Description: | 4.2 g in 1 APPLICATOR (54473-161-01) |
| NDC Code | 54473-161-01 |
| Proprietary Name | SUN SHADES |
| Package Description | 4.2 g in 1 APPLICATOR (54473-161-01) |
| Product NDC | 54473-161 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | octinoxate and oxybenzone |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20081001 |
| 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 |