espoir water splash sun serum

Generic: homosalate, octocrylene, octisalate, avobenzone

Labeler: espoir corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name espoir water splash sun serum
Generic Name homosalate, octocrylene, octisalate, avobenzone
Labeler espoir corporation
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

avobenzone 30 mg/mL, homosalate 95 mg/mL, octisalate 45 mg/mL, octocrylene 50 mg/mL

Manufacturer
ESPOIR Corporation

Identifiers & Regulatory

Product NDC 84469-721
Product ID 84469-721_3f724e4a-a6d4-f837-e063-6394a90ac084
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2024-09-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 84469721
Hyphenated Format 84469-721

Supplemental Identifiers

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 espoir water splash sun serum (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
  • 95 mg/mL
  • 45 mg/mL
  • 50 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, PUMP in 1 BOX (84469-721-01) / 50 mL in 1 BOTTLE, PUMP
  • 2 BOX in 1 BLISTER PACK (84469-721-03) / 1 BOTTLE, PUMP in 1 BOX / 50 mL in 1 BOTTLE, PUMP
source: ndc

Packages (2)

84469-721-01 1 BOTTLE, PUMP in 1 BOX (84469-721-01) / 50 mL in 1 BOTTLE, PUMP 84469-721-03 2 BOX in 1 BLISTER PACK (84469-721-03) / 1 BOTTLE, PUMP in 1 BOX / 50 mL in 1 BOTTLE, PUMP

Ingredients (4)

avobenzone (30 mg/mL) homosalate (95 mg/mL) octisalate (45 mg/mL) octocrylene (50 mg/mL)

Linked Drug Pages (1)

ESPOIR WATER SPLASH SUN SERUM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "3f724e4a-a6d4-f837-e063-6394a90ac084", "openfda": {"unii": ["G63QQF2NOX", "V06SV4M95S", "4X49Y0596W", "5A68WGF6WM"], "spl_set_id": ["1c4e7ba2-05e8-f949-e063-6394a90a699d"], "manufacturer_name": ["ESPOIR Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PUMP in 1 BOX (84469-721-01)  / 50 mL in 1 BOTTLE, PUMP", "package_ndc": "84469-721-01", "marketing_start_date": "20240902"}, {"sample": false, "description": "2 BOX in 1 BLISTER PACK (84469-721-03)  / 1 BOTTLE, PUMP in 1 BOX / 50 mL in 1 BOTTLE, PUMP", "package_ndc": "84469-721-03", "marketing_start_date": "20251201"}], "brand_name": "ESPOIR WATER SPLASH SUN SERUM", "product_id": "84469-721_3f724e4a-a6d4-f837-e063-6394a90ac084", "dosage_form": "LOTION", "product_ndc": "84469-721", "generic_name": "homosalate, octocrylene, octisalate, avobenzone", "labeler_name": "ESPOIR Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ESPOIR WATER SPLASH SUN SERUM", "active_ingredients": [{"name": "AVOBENZONE", "strength": "30 mg/mL"}, {"name": "HOMOSALATE", "strength": "95 mg/mL"}, {"name": "OCTISALATE", "strength": "45 mg/mL"}, {"name": "OCTOCRYLENE", "strength": "50 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240902", "listing_expiration_date": "20261231"}