cetaphil daily facial moisturizer with suncreen spf 50

Generic: octinoxate, octisalate, octocrylene, oxybenzone, titanium dioxide

Labeler: galderma laboratories, l.p.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name cetaphil daily facial moisturizer with suncreen spf 50
Generic Name octinoxate, octisalate, octocrylene, oxybenzone, titanium dioxide
Labeler galderma laboratories, l.p.
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

octinoxate 75 mg/mL, octisalate 50 mg/mL, octocrylene 70 mg/mL, oxybenzone 60 mg/mL, titanium dioxide 57 mg/mL

Manufacturer
Galderma Laboratories, L.P.

Identifiers & Regulatory

Product NDC 0299-4930
Product ID 0299-4930_0a1d0295-47d8-41f4-aaeb-5692637df0f1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2012-01-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02994930
Hyphenated Format 0299-4930

Supplemental Identifiers

UNII
4Y5P7MUD51 4X49Y0596W 5A68WGF6WM 95OOS7VE0Y 15FIX9V2JP

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 cetaphil daily facial moisturizer with suncreen spf 50 (source: ndc)
Generic Name octinoxate, octisalate, octocrylene, oxybenzone, titanium dioxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/mL
  • 50 mg/mL
  • 70 mg/mL
  • 60 mg/mL
  • 57 mg/mL
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (0299-4930-02) / 50 mL in 1 TUBE
source: ndc

Packages (1)

0299-4930-02 1 TUBE in 1 CARTON (0299-4930-02) / 50 mL in 1 TUBE

Ingredients (5)

octinoxate (75 mg/mL) octisalate (50 mg/mL) octocrylene (70 mg/mL) oxybenzone (60 mg/mL) titanium dioxide (57 mg/mL)

Linked Drug Pages (1)

Cetaphil Daily Facial Moisturizer with suncreen SPF 50 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "0a1d0295-47d8-41f4-aaeb-5692637df0f1", "openfda": {"unii": ["4Y5P7MUD51", "4X49Y0596W", "5A68WGF6WM", "95OOS7VE0Y", "15FIX9V2JP"], "spl_set_id": ["6650d137-e69e-4ec2-8311-3de74bf21315"], "manufacturer_name": ["Galderma Laboratories, L.P."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0299-4930-02)  / 50 mL in 1 TUBE", "package_ndc": "0299-4930-02", "marketing_start_date": "20120101"}], "brand_name": "Cetaphil Daily Facial Moisturizer with suncreen SPF 50", "product_id": "0299-4930_0a1d0295-47d8-41f4-aaeb-5692637df0f1", "dosage_form": "LOTION", "product_ndc": "0299-4930", "generic_name": "octinoxate, octisalate, octocrylene, oxybenzone, titanium dioxide", "labeler_name": "Galderma Laboratories, L.P.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetaphil Daily Facial Moisturizer with suncreen SPF 50", "active_ingredients": [{"name": "OCTINOXATE", "strength": "75 mg/mL"}, {"name": "OCTISALATE", "strength": "50 mg/mL"}, {"name": "OCTOCRYLENE", "strength": "70 mg/mL"}, {"name": "OXYBENZONE", "strength": "60 mg/mL"}, {"name": "TITANIUM DIOXIDE", "strength": "57 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120101", "listing_expiration_date": "20261231"}