Product NDC: | 50021-144 |
Proprietary Name: | SUNZONE FAMILY SUNSCREEN SPF 30 |
Non Proprietary Name: | Octinoxate, Octocrylene, Octisalate, Oxybenzone, Avobenzone and Homosalate. |
Active Ingredient(s): | 4.59; 2.4; 11.48; 7.65; 11.48; 6.12 g/153g; g/153g; g/153g; g/153g; g/153g; g/153g & nbsp; Octinoxate, Octocrylene, Octisalate, Oxybenzone, Avobenzone and Homosalate. |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50021-144 |
Labeler Name: | Empack Spraytech Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121108 |
Package NDC: | 50021-144-01 |
Package Description: | 153 g in 1 CAN (50021-144-01) |
NDC Code | 50021-144-01 |
Proprietary Name | SUNZONE FAMILY SUNSCREEN SPF 30 |
Package Description | 153 g in 1 CAN (50021-144-01) |
Product NDC | 50021-144 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Octocrylene, Octisalate, Oxybenzone, Avobenzone and Homosalate. |
Dosage Form Name | AEROSOL, SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20121108 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Empack Spraytech Inc. |
Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 4.59; 2.4; 11.48; 7.65; 11.48; 6.12 |
Strength Unit | g/153g; g/153g; g/153g; g/153g; g/153g; g/153g |
Pharmaceutical Classes |