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Ultra Light Sunscreen Broad Spectrum SPF 50
Ultra Light Sunscreen Broad Spectrum SPF 50 - 57627-117-02 - (Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone)
Drug Information of Ultra Light Sunscreen Broad Spectrum SPF 50
| Product NDC: | 57627-117 |
| Proprietary Name: | Ultra Light Sunscreen Broad Spectrum SPF 50 |
| Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone |
| Active Ingredient(s): | 3.39; 11.3; 5.65; 3.11; 6.78 g/113g; g/113g; g/113g; g/113g; g/113g & nbsp; Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ultra Light Sunscreen Broad Spectrum SPF 50
| Product NDC: | 57627-117 |
| Labeler Name: | Merle Norman Cosmetics |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130329 |
Package Information of Ultra Light Sunscreen Broad Spectrum SPF 50
| Package NDC: | 57627-117-02 |
| Package Description: | 1 TUBE in 1 CARTON (57627-117-02) > 113 g in 1 TUBE (57627-117-01) |
NDC Information of Ultra Light Sunscreen Broad Spectrum SPF 50
| NDC Code | 57627-117-02 |
| Proprietary Name | Ultra Light Sunscreen Broad Spectrum SPF 50 |
| Package Description | 1 TUBE in 1 CARTON (57627-117-02) > 113 g in 1 TUBE (57627-117-01) |
| Product NDC | 57627-117 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130329 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Merle Norman Cosmetics |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 3.39; 11.3; 5.65; 3.11; 6.78 |
| Strength Unit | g/113g; g/113g; g/113g; g/113g; g/113g |
| Pharmaceutical Classes |
