intellishade original spf 45

Generic: octinoxate, octisalate, titanium dioxide, zinc oxide

Labeler: revision, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name intellishade original spf 45
Generic Name octinoxate, octisalate, titanium dioxide, zinc oxide
Labeler revision, llc
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

octinoxate 7.5 g/100g, octisalate 5 g/100g, titanium dioxide 3.5 g/100g, zinc oxide 3 g/100g

Manufacturer
Revision, LLC

Identifiers & Regulatory

Product NDC 64651-7749
Product ID 64651-7749_483911c8-9ba2-d8a0-e063-6394a90a2888
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2027-12-31
Marketing Start 2013-07-09

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 646517749
Hyphenated Format 64651-7749

Supplemental Identifiers

UPC
0640451095813
UNII
4Y5P7MUD51 4X49Y0596W 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 intellishade original spf 45 (source: ndc)
Generic Name octinoxate, octisalate, titanium dioxide, zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 7.5 g/100g
  • 5 g/100g
  • 3.5 g/100g
  • 3 g/100g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (64651-7749-1) / 48 g in 1 TUBE
  • 227 g in 1 TUBE (64651-7749-2)
  • 3 g in 1 TUBE (64651-7749-3)
source: ndc

Packages (3)

64651-7749-1 1 TUBE in 1 CARTON (64651-7749-1) / 48 g in 1 TUBE 64651-7749-2 227 g in 1 TUBE (64651-7749-2) 64651-7749-3 3 g in 1 TUBE (64651-7749-3)

Ingredients (4)

octinoxate (7.5 g/100g) octisalate (5 g/100g) titanium dioxide (3.5 g/100g) zinc oxide (3 g/100g)

Linked Drug Pages (1)

Intellishade Original SPF 45 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "483911c8-9ba2-d8a0-e063-6394a90a2888", "openfda": {"upc": ["0640451095813"], "unii": ["4Y5P7MUD51", "4X49Y0596W", "15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["e213a681-eb22-69c0-e053-2995a90a899e"], "manufacturer_name": ["Revision, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (64651-7749-1)  / 48 g in 1 TUBE", "package_ndc": "64651-7749-1", "marketing_start_date": "20130709"}, {"sample": false, "description": "227 g in 1 TUBE (64651-7749-2)", "package_ndc": "64651-7749-2", "marketing_start_date": "20130709"}, {"sample": true, "description": "3 g in 1 TUBE (64651-7749-3)", "package_ndc": "64651-7749-3", "marketing_start_date": "20130709"}], "brand_name": "Intellishade Original SPF 45", "product_id": "64651-7749_483911c8-9ba2-d8a0-e063-6394a90a2888", "dosage_form": "CREAM", "product_ndc": "64651-7749", "generic_name": "Octinoxate, Octisalate, Titanium Dioxide, Zinc Oxide", "labeler_name": "Revision, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Intellishade Original SPF 45", "active_ingredients": [{"name": "OCTINOXATE", "strength": "7.5 g/100g"}, {"name": "OCTISALATE", "strength": "5 g/100g"}, {"name": "TITANIUM DIOXIDE", "strength": "3.5 g/100g"}, {"name": "ZINC OXIDE", "strength": "3 g/100g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130709", "listing_expiration_date": "20271231"}