uv daily deep tint

Generic: octinoxate, zinc oxide sunscreen

Labeler: cp skin health group, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name uv daily deep tint
Generic Name octinoxate, zinc oxide sunscreen
Labeler cp skin health group, inc.
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

octinoxate 750 g/1000g, zinc oxide 900 g/1000g

Manufacturer
CP Skin Health Group, Inc.

Identifiers & Regulatory

Product NDC 72043-2920
Product ID 72043-2920_79386a40-776e-47d1-8909-88776673d1a9
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2024-05-09

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 720432920
Hyphenated Format 72043-2920

Supplemental Identifiers

UPC
0827854015291
UNII
4Y5P7MUD51 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 uv daily deep tint (source: ndc)
Generic Name octinoxate, zinc oxide sunscreen (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 750 g/1000g
  • 900 g/1000g
source: ndc
Packaging
  • 50 g in 1 BOTTLE (72043-2920-1)
  • 2 g in 1 PACKET (72043-2920-2)
source: ndc

Packages (2)

72043-2920-1 50 g in 1 BOTTLE (72043-2920-1) 72043-2920-2 2 g in 1 PACKET (72043-2920-2)

Ingredients (2)

octinoxate (750 g/1000g) zinc oxide (900 g/1000g)

Linked Drug Pages (1)

UV Daily Deep Tint ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "79386a40-776e-47d1-8909-88776673d1a9", "openfda": {"upc": ["0827854015291"], "unii": ["4Y5P7MUD51", "SOI2LOH54Z"], "spl_set_id": ["c12fa9a4-d7e5-46bf-9bfb-1cbbaa73b450"], "manufacturer_name": ["CP Skin Health Group, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 BOTTLE (72043-2920-1)", "package_ndc": "72043-2920-1", "marketing_start_date": "20240509"}, {"sample": false, "description": "2 g in 1 PACKET (72043-2920-2)", "package_ndc": "72043-2920-2", "marketing_start_date": "20240509"}], "brand_name": "UV Daily Deep Tint", "product_id": "72043-2920_79386a40-776e-47d1-8909-88776673d1a9", "dosage_form": "LOTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "72043-2920", "generic_name": "octinoxate, zinc oxide sunscreen", "labeler_name": "CP Skin Health Group, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "UV Daily Deep Tint", "active_ingredients": [{"name": "OCTINOXATE", "strength": "750 g/1000g"}, {"name": "ZINC OXIDE", "strength": "900 g/1000g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240509", "listing_expiration_date": "20261231"}