Home
>
National Drug Code (NDC)
>
SUNSCREEN
SUNSCREEN - 57367-029-05 - (HOMOSALATE OXYBENZONE OCTISALATE AVOBENZONE OCTYLCRYLENE)
Drug Information of SUNSCREEN
| Product NDC: | 57367-029 |
| Proprietary Name: | SUNSCREEN |
| Non Proprietary Name: | HOMOSALATE OXYBENZONE OCTISALATE AVOBENZONE OCTYLCRYLENE |
| Active Ingredient(s): | 30; 150; 50; 20; 50 mg/g; mg/g; mg/g; mg/g; mg/g & nbsp; HOMOSALATE OXYBENZONE OCTISALATE AVOBENZONE OCTYLCRYLENE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUNSCREEN
| Product NDC: | 57367-029 |
| Labeler Name: | 220 Laboratories Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100510 |
Package Information of SUNSCREEN
| Package NDC: | 57367-029-05 |
| Package Description: | 106 g in 1 CAN (57367-029-05) |
NDC Information of SUNSCREEN
| NDC Code | 57367-029-05 |
| Proprietary Name | SUNSCREEN |
| Package Description | 106 g in 1 CAN (57367-029-05) |
| Product NDC | 57367-029 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HOMOSALATE OXYBENZONE OCTISALATE AVOBENZONE OCTYLCRYLENE |
| Dosage Form Name | AEROSOL, SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20100510 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | 220 Laboratories Inc |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 30; 150; 50; 20; 50 |
| Strength Unit | mg/g; mg/g; mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
