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ULTRASOL
ULTRASOL - 59886-353-66 - (Avobenzone, Octinoxate, Octisalate, Octocrylene, Oxybenzone)
Drug Information of ULTRASOL
| Product NDC: | 59886-353 |
| Proprietary Name: | ULTRASOL |
| Non Proprietary Name: | Avobenzone, Octinoxate, Octisalate, Octocrylene, Oxybenzone |
| Active Ingredient(s): | 2; 7.5; 5; 9; 4 g/100g; g/100g; g/100g; g/100g; g/100g & nbsp; Avobenzone, Octinoxate, Octisalate, Octocrylene, Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ULTRASOL
| Product NDC: | 59886-353 |
| Labeler Name: | Fischer Pharmaceuticals Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100610 |
Package Information of ULTRASOL
| Package NDC: | 59886-353-66 |
| Package Description: | 200 g in 1 CAN (59886-353-66) |
NDC Information of ULTRASOL
| NDC Code | 59886-353-66 |
| Proprietary Name | ULTRASOL |
| Package Description | 200 g in 1 CAN (59886-353-66) |
| Product NDC | 59886-353 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, Octisalate, Octocrylene, Oxybenzone |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100610 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Fischer Pharmaceuticals Ltd. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 2; 7.5; 5; 9; 4 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
