sun veil illuminatingelixir face sunscreen spf 38

Generic: octisalate, octocrylene, zinc oxide

Labeler: koco life llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sun veil illuminatingelixir face sunscreen spf 38
Generic Name octisalate, octocrylene, zinc oxide
Labeler koco life llc
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

octisalate 50 mg/mL, octocrylene 100 mg/mL, zinc oxide 150 mg/mL

Manufacturer
Koco Life LLC

Identifiers & Regulatory

Product NDC 84130-019
Product ID 84130-019_4a15c479-d677-9e52-e063-6394a90a4eb4
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2027-12-31
Marketing Start 2026-01-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 84130019
Hyphenated Format 84130-019

Supplemental Identifiers

UPC
0850068900909
UNII
4X49Y0596W 5A68WGF6WM 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 sun veil illuminatingelixir face sunscreen spf 38 (source: ndc)
Generic Name octisalate, octocrylene, zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/mL
  • 100 mg/mL
  • 150 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, DROPPER in 1 CARTON (84130-019-12) / 30 mL in 1 BOTTLE, DROPPER (84130-019-11)
  • 8 mL in 1 TUBE (84130-019-20)
source: ndc

Packages (2)

84130-019-12 1 BOTTLE, DROPPER in 1 CARTON (84130-019-12) / 30 mL in 1 BOTTLE, DROPPER (84130-019-11) 84130-019-20 8 mL in 1 TUBE (84130-019-20)

Ingredients (3)

octisalate (50 mg/mL) octocrylene (100 mg/mL) zinc oxide (150 mg/mL)

Linked Drug Pages (1)

Sun Veil IlluminatingElixir Face Sunscreen SPF 38 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4a15c479-d677-9e52-e063-6394a90a4eb4", "openfda": {"upc": ["0850068900909"], "unii": ["4X49Y0596W", "5A68WGF6WM", "SOI2LOH54Z"], "spl_set_id": ["4a15c479-d676-9e52-e063-6394a90a4eb4"], "manufacturer_name": ["Koco Life LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (84130-019-12)  / 30 mL in 1 BOTTLE, DROPPER (84130-019-11)", "package_ndc": "84130-019-12", "marketing_start_date": "20260115"}, {"sample": false, "description": "8 mL in 1 TUBE (84130-019-20)", "package_ndc": "84130-019-20", "marketing_start_date": "20260115"}], "brand_name": "Sun Veil IlluminatingElixir Face Sunscreen SPF 38", "product_id": "84130-019_4a15c479-d677-9e52-e063-6394a90a4eb4", "dosage_form": "LOTION", "product_ndc": "84130-019", "generic_name": "Octisalate, Octocrylene, Zinc Oxide", "labeler_name": "Koco Life LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sun Veil IlluminatingElixir Face Sunscreen SPF 38", "active_ingredients": [{"name": "OCTISALATE", "strength": "50 mg/mL"}, {"name": "OCTOCRYLENE", "strength": "100 mg/mL"}, {"name": "ZINC OXIDE", "strength": "150 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20260115", "listing_expiration_date": "20271231"}