mary kay cc cream sunscreen broad spectrum spf 15 very light

Generic: homosalate, octinoxate, oxybenzone

Labeler: mary kay inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mary kay cc cream sunscreen broad spectrum spf 15 very light
Generic Name homosalate, octinoxate, oxybenzone
Labeler mary kay inc.
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

homosalate 5 g/100mL, octinoxate 6.5 g/100mL, oxybenzone 1.2 g/100mL

Manufacturer
Mary Kay Inc.

Identifiers & Regulatory

Product NDC 51531-2822
Product ID 51531-2822_297a27f1-0898-38aa-e063-6394a90adea1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2014-02-16

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 515312822
Hyphenated Format 51531-2822

Supplemental Identifiers

UNII
V06SV4M95S 4Y5P7MUD51 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 mary kay cc cream sunscreen broad spectrum spf 15 very light (source: ndc)
Generic Name homosalate, octinoxate, oxybenzone (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 5 g/100mL
  • 6.5 g/100mL
  • 1.2 g/100mL
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (51531-2822-1) / 29 mL in 1 TUBE
  • 1 mL in 1 PACKET (51531-2822-3)
source: ndc

Packages (2)

51531-2822-1 1 TUBE in 1 CARTON (51531-2822-1) / 29 mL in 1 TUBE 51531-2822-3 1 mL in 1 PACKET (51531-2822-3)

Ingredients (3)

homosalate (5 g/100mL) octinoxate (6.5 g/100mL) oxybenzone (1.2 g/100mL)

Linked Drug Pages (1)

Mary Kay CC Cream Sunscreen Broad Spectrum SPF 15 Very Light ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "297a27f1-0898-38aa-e063-6394a90adea1", "openfda": {"unii": ["V06SV4M95S", "4Y5P7MUD51", "95OOS7VE0Y"], "spl_set_id": ["af22b3a5-ac72-4c2a-aa7e-6b5ca07d89e8"], "manufacturer_name": ["Mary Kay Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51531-2822-1)  / 29 mL in 1 TUBE", "package_ndc": "51531-2822-1", "marketing_start_date": "20140216"}, {"sample": true, "description": "1 mL in 1 PACKET (51531-2822-3)", "package_ndc": "51531-2822-3", "marketing_start_date": "20140216"}], "brand_name": "Mary Kay CC Cream Sunscreen Broad Spectrum SPF 15 Very Light", "product_id": "51531-2822_297a27f1-0898-38aa-e063-6394a90adea1", "dosage_form": "CREAM", "product_ndc": "51531-2822", "generic_name": "homosalate, octinoxate, oxybenzone", "labeler_name": "Mary Kay Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mary Kay CC Cream Sunscreen Broad Spectrum SPF 15 Very Light", "active_ingredients": [{"name": "HOMOSALATE", "strength": "5 g/100mL"}, {"name": "OCTINOXATE", "strength": "6.5 g/100mL"}, {"name": "OXYBENZONE", "strength": "1.2 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140216", "listing_expiration_date": "20261231"}