Search by Drug Name or NDC
NDC 71501-1903-01 Universal Glow Daily Defense SPF 40 170 mg/mL Details
Universal Glow Daily Defense SPF 40 170 mg/mL
Universal Glow Daily Defense 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 SALICYLIC ACID.
Product Information
| NDC | 71501-1903 |
|---|---|
| Product ID | 71501-1903_fae21e0a-5e42-bffb-e053-6294a90afb9d |
| 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 | Universal Glow Daily Defense SPF 40 |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Zinc Oxide |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | CREAM |
| Route | TOPICAL |
| Active Ingredient Strength | 170 |
| Active Ingredient Units | mg/mL |
| Substance Name | SALICYLIC ACID |
| Labeler Name | Dr. Loretta, LLC |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | M020 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 71501-1903-01 (71501190301)
| NDC Package Code | 71501-1903-1 |
|---|---|
| Billing NDC | 71501190301 |
| Package | 50 mL in 1 TUBE (71501-1903-1) |
| Marketing Start Date | 2023-05-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |