standard procedure spf 50 sunscreen

Generic: homosalate, octocrylene, octisalate, avobenzone

Labeler: standard procedure inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name standard procedure spf 50 sunscreen
Generic Name homosalate, octocrylene, octisalate, avobenzone
Labeler standard procedure inc
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

avobenzone 30 mg/mL, homosalate 100 mg/mL, octisalate 50 mg/mL, octocrylene 80 mg/mL

Manufacturer
Standard Procedure Inc

Identifiers & Regulatory

Product NDC 84425-101
Product ID 84425-101_4862fbef-e8ad-cc4b-e063-6394a90a35f2
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2027-12-31
Marketing Start 2024-07-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 84425101
Hyphenated Format 84425-101

Supplemental Identifiers

UPC
9358579000091
UNII
G63QQF2NOX V06SV4M95S 4X49Y0596W 5A68WGF6WM

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 standard procedure spf 50 sunscreen (source: ndc)
Generic Name homosalate, octocrylene, octisalate, avobenzone (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/mL
  • 100 mg/mL
  • 50 mg/mL
  • 80 mg/mL
source: ndc
Packaging
  • 60 mL in 1 BOTTLE, PLASTIC (84425-101-01)
  • 250 mL in 1 BOTTLE, PLASTIC (84425-101-03)
  • 500 mL in 1 BOTTLE, PLASTIC (84425-101-04)
source: ndc

Packages (3)

84425-101-01 60 mL in 1 BOTTLE, PLASTIC (84425-101-01) 84425-101-03 250 mL in 1 BOTTLE, PLASTIC (84425-101-03) 84425-101-04 500 mL in 1 BOTTLE, PLASTIC (84425-101-04)

Ingredients (4)

avobenzone (30 mg/mL) homosalate (100 mg/mL) octisalate (50 mg/mL) octocrylene (80 mg/mL)

Linked Drug Pages (1)

Standard Procedure SPF 50 Sunscreen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4862fbef-e8ad-cc4b-e063-6394a90a35f2", "openfda": {"upc": ["9358579000091"], "unii": ["G63QQF2NOX", "V06SV4M95S", "4X49Y0596W", "5A68WGF6WM"], "spl_set_id": ["1d3f87de-90c0-75c0-e063-6394a90a2ef4"], "manufacturer_name": ["Standard Procedure Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 mL in 1 BOTTLE, PLASTIC (84425-101-01)", "package_ndc": "84425-101-01", "marketing_start_date": "20240715"}, {"sample": false, "description": "250 mL in 1 BOTTLE, PLASTIC (84425-101-03)", "package_ndc": "84425-101-03", "marketing_start_date": "20240715"}, {"sample": false, "description": "500 mL in 1 BOTTLE, PLASTIC (84425-101-04)", "package_ndc": "84425-101-04", "marketing_start_date": "20240715"}], "brand_name": "Standard Procedure SPF 50 Sunscreen", "product_id": "84425-101_4862fbef-e8ad-cc4b-e063-6394a90a35f2", "dosage_form": "LOTION", "product_ndc": "84425-101", "generic_name": "Homosalate, Octocrylene, Octisalate, Avobenzone", "labeler_name": "Standard Procedure Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Standard Procedure SPF 50 Sunscreen", "active_ingredients": [{"name": "AVOBENZONE", "strength": "30 mg/mL"}, {"name": "HOMOSALATE", "strength": "100 mg/mL"}, {"name": "OCTISALATE", "strength": "50 mg/mL"}, {"name": "OCTOCRYLENE", "strength": "80 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240715", "listing_expiration_date": "20271231"}