estee lauder multi-defense aqua uv gel broad spectrum spf 50

Generic: avobenzone, homosalate, octisalate, octocrylene, and oxybenzone

Labeler: estee lauder inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name estee lauder multi-defense aqua uv gel broad spectrum spf 50
Generic Name avobenzone, homosalate, octisalate, octocrylene, and oxybenzone
Labeler estee lauder inc
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

avobenzone 30 mg/mL, homosalate 50 mg/mL, octisalate 45 mg/mL, octocrylene 28 mg/mL, oxybenzone 30 mg/mL

Manufacturer
ESTEE LAUDER INC

Identifiers & Regulatory

Product NDC 11559-060
Product ID 11559-060_2a15b78c-0356-b0b0-e063-6294a90a09db
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2020-05-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11559060
Hyphenated Format 11559-060

Supplemental Identifiers

UNII
G63QQF2NOX V06SV4M95S 4X49Y0596W 5A68WGF6WM 95OOS7VE0Y

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 estee lauder multi-defense aqua uv gel broad spectrum spf 50 (source: ndc)
Generic Name avobenzone, homosalate, octisalate, octocrylene, and oxybenzone (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/mL
  • 50 mg/mL
  • 45 mg/mL
  • 28 mg/mL
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (11559-060-01) / 30 mL in 1 TUBE
source: ndc

Packages (1)

11559-060-01 1 TUBE in 1 CARTON (11559-060-01) / 30 mL in 1 TUBE

Ingredients (5)

avobenzone (30 mg/mL) homosalate (50 mg/mL) octisalate (45 mg/mL) octocrylene (28 mg/mL) oxybenzone (30 mg/mL)

Linked Drug Pages (1)

ESTEE LAUDER MULTI-DEFENSE AQUA UV gel BROAD SPECTRUM SPF 50 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2a15b78c-0356-b0b0-e063-6294a90a09db", "openfda": {"unii": ["G63QQF2NOX", "V06SV4M95S", "4X49Y0596W", "5A68WGF6WM", "95OOS7VE0Y"], "spl_set_id": ["0770e251-95d0-43de-88f1-bc0a29811e4e"], "manufacturer_name": ["ESTEE LAUDER INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (11559-060-01)  / 30 mL in 1 TUBE", "package_ndc": "11559-060-01", "marketing_start_date": "20200508"}], "brand_name": "ESTEE LAUDER MULTI-DEFENSE AQUA UV gel BROAD SPECTRUM SPF 50", "product_id": "11559-060_2a15b78c-0356-b0b0-e063-6294a90a09db", "dosage_form": "LOTION", "product_ndc": "11559-060", "generic_name": "AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE", "labeler_name": "ESTEE LAUDER INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ESTEE LAUDER MULTI-DEFENSE AQUA UV gel BROAD SPECTRUM SPF 50", "active_ingredients": [{"name": "AVOBENZONE", "strength": "30 mg/mL"}, {"name": "HOMOSALATE", "strength": "50 mg/mL"}, {"name": "OCTISALATE", "strength": "45 mg/mL"}, {"name": "OCTOCRYLENE", "strength": "28 mg/mL"}, {"name": "OXYBENZONE", "strength": "30 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200504", "listing_expiration_date": "20261231"}