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NDC 71501-1902-01 Urban Antioxidant Sunscreen SPF 40 80; 50; 50; 80 mg/mL; mg/mL; mg/mL; mg/mL Details
Urban Antioxidant Sunscreen SPF 40 80; 50; 50; 80 mg/mL; mg/mL; mg/mL; mg/mL
Urban Antioxidant Sunscreen SPF 40 is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by Dr. Loretta, LLC. The primary component is HOMOSALATE; OCTISALATE; OCTOCRYLENE; ZINC OXIDE.
Product Information
NDC | 71501-1902 |
---|---|
Product ID | 71501-1902_0c868857-d5b1-9413-e063-6294a90a0bab |
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 | Urban Antioxidant Sunscreen SPF 40 |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Homosalate, Octisalate, Octocrylene, Zinc Oxyide cream |
Product Type | HUMAN OTC DRUG |
Dosage Form | CREAM |
Route | TOPICAL |
Active Ingredient Strength | 80; 50; 50; 80 |
Active Ingredient Units | mg/mL; mg/mL; mg/mL; mg/mL |
Substance Name | HOMOSALATE; OCTISALATE; OCTOCRYLENE; ZINC OXIDE |
Labeler Name | Dr. Loretta, LLC |
Pharmaceutical Class | n/a |
DEA Schedule | n/a |
Marketing Category | OTC MONOGRAPH DRUG |
Application Number | M020 |
Listing Certified Through | 2024-12-31 |
Package
NDC 71501-1902-01 (71501190201)
NDC Package Code | 71501-1902-1 |
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Billing NDC | 71501190201 |
Package | 50 mL in 1 BOTTLE, PLASTIC (71501-1902-1) |
Marketing Start Date | 2019-09-16 |
NDC Exclude Flag | N |
Pricing Information | N/A |