clinique super defense city block daily energy plus face protector broad spectrum spf 50

Generic: octinoxate, titanium dioxide, and zinc oxide

Labeler: clinique laboratories llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name clinique super defense city block daily energy plus face protector broad spectrum spf 50
Generic Name octinoxate, titanium dioxide, and zinc oxide
Labeler clinique laboratories llc
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

octinoxate 50 mg/mL, titanium dioxide 32 mg/mL, zinc oxide 36 mg/mL

Manufacturer
CLINIQUE LABORATORIES LLC

Identifiers & Regulatory

Product NDC 49527-078
Product ID 49527-078_2a14d49c-42c5-7aca-e063-6394a90a25aa
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2020-06-25

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49527078
Hyphenated Format 49527-078

Supplemental Identifiers

UNII
4Y5P7MUD51 15FIX9V2JP 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 clinique super defense city block daily energy plus face protector broad spectrum spf 50 (source: ndc)
Generic Name octinoxate, titanium dioxide, and zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/mL
  • 32 mg/mL
  • 36 mg/mL
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (49527-078-01) / 40 mL in 1 TUBE
source: ndc

Packages (1)

49527-078-01 1 TUBE in 1 CARTON (49527-078-01) / 40 mL in 1 TUBE

Ingredients (3)

octinoxate (50 mg/mL) titanium dioxide (32 mg/mL) zinc oxide (36 mg/mL)

Linked Drug Pages (1)

CLINIQUE SUPER DEFENSE CITY BLOCK DAILY ENERGY PLUS FACE PROTECTOR BROAD SPECTRUM SPF 50 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2a14d49c-42c5-7aca-e063-6394a90a25aa", "openfda": {"unii": ["4Y5P7MUD51", "15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["d1a3d76f-16dd-4533-8144-9a3175f6e15f"], "manufacturer_name": ["CLINIQUE LABORATORIES LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (49527-078-01)  / 40 mL in 1 TUBE", "package_ndc": "49527-078-01", "marketing_start_date": "20200625"}], "brand_name": "CLINIQUE SUPER DEFENSE CITY BLOCK DAILY ENERGY PLUS FACE PROTECTOR BROAD SPECTRUM SPF 50", "product_id": "49527-078_2a14d49c-42c5-7aca-e063-6394a90a25aa", "dosage_form": "LOTION", "product_ndc": "49527-078", "generic_name": "OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDE", "labeler_name": "CLINIQUE LABORATORIES LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CLINIQUE SUPER DEFENSE CITY BLOCK DAILY ENERGY PLUS FACE PROTECTOR BROAD SPECTRUM SPF 50", "active_ingredients": [{"name": "OCTINOXATE", "strength": "50 mg/mL"}, {"name": "TITANIUM DIOXIDE", "strength": "32 mg/mL"}, {"name": "ZINC OXIDE", "strength": "36 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200625", "listing_expiration_date": "20261231"}