dr loretta universal glow daily defense spf 40

Generic: zinc oxide

Labeler: dr. loretta, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name dr loretta universal glow daily defense spf 40
Generic Name zinc oxide
Labeler dr. loretta, llc
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

zinc oxide 170 mg/mL

Manufacturer
Dr. Loretta, LLC

Identifiers & Regulatory

Product NDC 71501-1904
Product ID 71501-1904_2de40ee1-ec9e-a4fc-e063-6294a90a7cb1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2025-02-05

Pharmacologic Class

Classes
copper absorption inhibitor [epc] decreased copper ion absorption [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 715011904
Hyphenated Format 71501-1904

Supplemental Identifiers

UPC
0185854000434
UNII
SOI2LOH54Z

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name dr loretta universal glow daily defense spf 40 (source: ndc)
Generic Name zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 170 mg/mL
source: ndc
Packaging
  • 50 mL in 1 TUBE, WITH APPLICATOR (71501-1904-1)
source: ndc

Packages (1)

71501-1904-1 50 mL in 1 TUBE, WITH APPLICATOR (71501-1904-1)

Ingredients (1)

zinc oxide (170 mg/mL)

Linked Drug Pages (1)

Dr Loretta Universal Glow Daily Defense SPF 40 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2de40ee1-ec9e-a4fc-e063-6294a90a7cb1", "openfda": {"upc": ["0185854000434"], "unii": ["SOI2LOH54Z"], "spl_set_id": ["ebdaf6c1-1572-4840-851b-6d780471fcb2"], "manufacturer_name": ["Dr. Loretta, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 TUBE, WITH APPLICATOR (71501-1904-1)", "package_ndc": "71501-1904-1", "marketing_start_date": "20250205"}], "brand_name": "Dr Loretta Universal Glow Daily Defense SPF 40", "product_id": "71501-1904_2de40ee1-ec9e-a4fc-e063-6294a90a7cb1", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "71501-1904", "generic_name": "ZINC OXIDE", "labeler_name": "Dr. Loretta, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dr Loretta Universal Glow Daily Defense SPF 40", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "170 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250205", "listing_expiration_date": "20261231"}