neostrata enlighten skin brightener with sunscreen broad spectrum spf 35

Generic: octinoxate, octisalate, and avobenzone

Labeler: neostrata company inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name neostrata enlighten skin brightener with sunscreen broad spectrum spf 35
Generic Name octinoxate, octisalate, and avobenzone
Labeler neostrata company inc.
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

avobenzone 30 mg/g, octinoxate 75 mg/g, octisalate 50 mg/g

Manufacturer
NeoStrata Company Inc.

Identifiers & Regulatory

Product NDC 58414-0019
Product ID 58414-0019_2b59538b-e516-a18d-e063-6394a90aeeab
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2018-12-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 584140019
Hyphenated Format 58414-0019

Supplemental Identifiers

UPC
0732013301316
UNII
G63QQF2NOX 4Y5P7MUD51 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 neostrata enlighten skin brightener with sunscreen broad spectrum spf 35 (source: ndc)
Generic Name octinoxate, octisalate, and avobenzone (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/g
  • 75 mg/g
  • 50 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (58414-0019-1) / 40 g in 1 TUBE
source: ndc

Packages (1)

58414-0019-1 1 TUBE in 1 CARTON (58414-0019-1) / 40 g in 1 TUBE

Ingredients (3)

avobenzone (30 mg/g) octinoxate (75 mg/g) octisalate (50 mg/g)

Linked Drug Pages (1)

NeoStrata Enlighten Skin Brightener with Sunscreen Broad Spectrum SPF 35 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2b59538b-e516-a18d-e063-6394a90aeeab", "openfda": {"upc": ["0732013301316"], "unii": ["G63QQF2NOX", "4Y5P7MUD51", "4X49Y0596W"], "spl_set_id": ["ed495f18-2f8e-4991-b797-82e9f6fc7acb"], "manufacturer_name": ["NeoStrata Company Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (58414-0019-1)  / 40 g in 1 TUBE", "package_ndc": "58414-0019-1", "marketing_start_date": "20181201"}], "brand_name": "NeoStrata Enlighten Skin Brightener with Sunscreen Broad Spectrum SPF 35", "product_id": "58414-0019_2b59538b-e516-a18d-e063-6394a90aeeab", "dosage_form": "CREAM", "product_ndc": "58414-0019", "generic_name": "Octinoxate, Octisalate, and Avobenzone", "labeler_name": "NeoStrata Company Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NeoStrata Enlighten Skin Brightener", "brand_name_suffix": "with Sunscreen Broad Spectrum SPF 35", "active_ingredients": [{"name": "AVOBENZONE", "strength": "30 mg/g"}, {"name": "OCTINOXATE", "strength": "75 mg/g"}, {"name": "OCTISALATE", "strength": "50 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20181201", "listing_expiration_date": "20261231"}