summer gelee spf-4

Generic: homosalate, octisalate

Labeler: summer gelee llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name summer gelee spf-4
Generic Name homosalate, octisalate
Labeler summer gelee llc
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

homosalate 20 mg/mL, octisalate 20 mg/mL

Manufacturer
SUMMER GELEE LLC

Identifiers & Regulatory

Product NDC 84281-476
Product ID 84281-476_171b4cde-2e02-0bb4-e063-6394a90a9deb
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2024-05-06

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 84281476
Hyphenated Format 84281-476

Supplemental Identifiers

UNII
V06SV4M95S 4X49Y0596W

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 summer gelee spf-4 (source: ndc)
Generic Name homosalate, octisalate (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 92.26 mL in 1 TUBE (84281-476-00)
source: ndc

Packages (1)

84281-476-00 92.26 mL in 1 TUBE (84281-476-00)

Ingredients (2)

homosalate (20 mg/mL) octisalate (20 mg/mL)

Linked Drug Pages (1)

SUMMER GELEE SPF-4 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "171b4cde-2e02-0bb4-e063-6394a90a9deb", "openfda": {"unii": ["V06SV4M95S", "4X49Y0596W"], "spl_set_id": ["c9ec81ad-0478-4026-bc6c-5582eb012b8d"], "manufacturer_name": ["SUMMER GELEE LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "92.26 mL in 1 TUBE (84281-476-00)", "package_ndc": "84281-476-00", "marketing_start_date": "20240506"}], "brand_name": "SUMMER GELEE SPF-4", "product_id": "84281-476_171b4cde-2e02-0bb4-e063-6394a90a9deb", "dosage_form": "GEL", "product_ndc": "84281-476", "generic_name": "HOMOSALATE, OCTISALATE", "labeler_name": "SUMMER GELEE LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SUMMER GELEE SPF-4", "active_ingredients": [{"name": "HOMOSALATE", "strength": "20 mg/mL"}, {"name": "OCTISALATE", "strength": "20 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240506", "listing_expiration_date": "20261231"}