coretex sun x spf 30 thin

Generic: avobenzone, homosalate, octinoxate, octisalate, oxybenzone

Labeler: coretex products inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name coretex sun x spf 30 thin
Generic Name avobenzone, homosalate, octinoxate, octisalate, oxybenzone
Labeler coretex products inc
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

avobenzone 1 g/100mL, homosalate 5 g/100mL, octinoxate 7.5 g/100mL, octisalate 5 g/100mL, oxybenzone 6 g/100mL

Manufacturer
CoreTex Products Inc

Identifiers & Regulatory

Product NDC 65753-101
Product ID 65753-101_0847f22b-ece4-e4c1-e063-6394a90a4d62
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2018-11-22

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65753101
Hyphenated Format 65753-101

Supplemental Identifiers

UPC
0698229716613
UNII
G63QQF2NOX V06SV4M95S 4Y5P7MUD51 4X49Y0596W 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 coretex sun x spf 30 thin (source: ndc)
Generic Name avobenzone, homosalate, octinoxate, octisalate, oxybenzone (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1 g/100mL
  • 5 g/100mL
  • 7.5 g/100mL
  • 6 g/100mL
source: ndc
Packaging
  • 59 mL in 1 BOTTLE, SPRAY (65753-101-11)
  • 118 mL in 1 BOTTLE, SPRAY (65753-101-12)
source: ndc

Packages (2)

65753-101-11 59 mL in 1 BOTTLE, SPRAY (65753-101-11) 65753-101-12 118 mL in 1 BOTTLE, SPRAY (65753-101-12)

Ingredients (5)

avobenzone (1 g/100mL) homosalate (5 g/100mL) octinoxate (7.5 g/100mL) octisalate (5 g/100mL) oxybenzone (6 g/100mL)

Linked Drug Pages (1)

CoreTex Sun X SPF 30 Thin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "0847f22b-ece4-e4c1-e063-6394a90a4d62", "openfda": {"upc": ["0698229716613"], "unii": ["G63QQF2NOX", "V06SV4M95S", "4Y5P7MUD51", "4X49Y0596W", "95OOS7VE0Y"], "spl_set_id": ["980388b5-8314-3143-e053-2995a90a7288"], "manufacturer_name": ["CoreTex Products Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE, SPRAY (65753-101-11)", "package_ndc": "65753-101-11", "marketing_start_date": "20191122"}, {"sample": false, "description": "118 mL in 1 BOTTLE, SPRAY (65753-101-12)", "package_ndc": "65753-101-12", "marketing_start_date": "20191122"}], "brand_name": "CoreTex Sun X SPF 30 Thin", "product_id": "65753-101_0847f22b-ece4-e4c1-e063-6394a90a4d62", "dosage_form": "LIQUID", "product_ndc": "65753-101", "generic_name": "Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone", "labeler_name": "CoreTex Products Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CoreTex Sun X SPF 30 Thin", "active_ingredients": [{"name": "AVOBENZONE", "strength": "1 g/100mL"}, {"name": "HOMOSALATE", "strength": "5 g/100mL"}, {"name": "OCTINOXATE", "strength": "7.5 g/100mL"}, {"name": "OCTISALATE", "strength": "5 g/100mL"}, {"name": "OXYBENZONE", "strength": "6 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20181122", "listing_expiration_date": "20261231"}