shiseido future solution lx total protective

Generic: avobenzone, octinoxate, octocrylene, and oxybenzone

Labeler: shiseido americas corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name shiseido future solution lx total protective
Generic Name avobenzone, octinoxate, octocrylene, and oxybenzone
Labeler shiseido americas corporation
Dosage Form EMULSION
Routes
TOPICAL
Active Ingredients

avobenzone 1136 mg/75mL, octinoxate 5606 mg/75mL, octocrylene 1515 mg/75mL, oxybenzone 758 mg/75mL

Manufacturer
SHISEIDO AMERICAS CORPORATION

Identifiers & Regulatory

Product NDC 58411-327
Product ID 58411-327_47ab9609-4282-30b2-e063-6394a90a421e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2027-12-31
Marketing Start 2017-08-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58411327
Hyphenated Format 58411-327

Supplemental Identifiers

UNII
G63QQF2NOX 4Y5P7MUD51 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 shiseido future solution lx total protective (source: ndc)
Generic Name avobenzone, octinoxate, octocrylene, and oxybenzone (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1136 mg/75mL
  • 5606 mg/75mL
  • 1515 mg/75mL
  • 758 mg/75mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (58411-327-10) / 75 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

58411-327-10 1 BOTTLE, PLASTIC in 1 CARTON (58411-327-10) / 75 mL in 1 BOTTLE, PLASTIC

Ingredients (4)

avobenzone (1136 mg/75mL) octinoxate (5606 mg/75mL) octocrylene (1515 mg/75mL) oxybenzone (758 mg/75mL)

Linked Drug Pages (1)

Shiseido Future Solution LX Total Protective ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "47ab9609-4282-30b2-e063-6394a90a421e", "openfda": {"unii": ["G63QQF2NOX", "4Y5P7MUD51", "5A68WGF6WM", "95OOS7VE0Y"], "spl_set_id": ["6de17911-4bce-46c9-906b-07d899a36ceb"], "manufacturer_name": ["SHISEIDO AMERICAS CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (58411-327-10)  / 75 mL in 1 BOTTLE, PLASTIC", "package_ndc": "58411-327-10", "marketing_start_date": "20170801"}], "brand_name": "Shiseido Future Solution LX Total Protective", "product_id": "58411-327_47ab9609-4282-30b2-e063-6394a90a421e", "dosage_form": "EMULSION", "product_ndc": "58411-327", "generic_name": "AVOBENZONE, OCTINOXATE, OCTOCRYLENE, and OXYBENZONE", "labeler_name": "SHISEIDO AMERICAS CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Shiseido Future Solution LX Total Protective", "active_ingredients": [{"name": "AVOBENZONE", "strength": "1136 mg/75mL"}, {"name": "OCTINOXATE", "strength": "5606 mg/75mL"}, {"name": "OCTOCRYLENE", "strength": "1515 mg/75mL"}, {"name": "OXYBENZONE", "strength": "758 mg/75mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170801", "listing_expiration_date": "20271231"}