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NDC 56152-4008-02 SPF 50 Face Sunscreen 3; 10; 7; 5; 5; 6 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL Details
SPF 50 Face Sunscreen 3; 10; 7; 5; 5; 6 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
SPF 50 Face Sunscreen is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by Cosmetic Enterprises Ltd. The primary component is AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE.
Product Information
| NDC | 56152-4008 |
|---|---|
| Product ID | 56152-4008_08184612-d897-f6ac-e063-6294a90a7afa |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | SPF 50 Face Sunscreen |
| Proprietary Name Suffix | Bioelements |
| Non-Proprietary Name | Avobenzone, Homosalate, Octinoxate, Octisalate, Octocrylene, Oxybenzone |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | CREAM |
| Route | TOPICAL |
| Active Ingredient Strength | 3; 10; 7; 5; 5; 6 |
| Active Ingredient Units | g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Labeler Name | Cosmetic Enterprises Ltd |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M020 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 56152-4008-02 (56152400802)
| NDC Package Code | 56152-4008-2 |
|---|---|
| Billing NDC | 56152400802 |
| Package | 1 TUBE in 1 BOX (56152-4008-2) / 68 mL in 1 TUBE (56152-4008-1) |
| Marketing Start Date | 2016-01-04 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |