Cetaphil Daily Facial Moisturizer with suncreen SPF 50

Product NDC: 0299-4930
11-digit product format: 002994930
Labeler code: 0299
Product ID: 0299-4930_0a1d0295-47d8-41f4-aaeb-5692637df0f1
Type: HUMAN OTC DRUG
Nonproprietary name: octinoxate, octisalate, octocrylene, oxybenzone, titanium dioxide
Dosage form: LOTION
Route: TOPICAL
Labeler: Galderma Laboratories, L.P.
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2012-01-01
Substance: OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE; TITANIUM DIOXIDE
Active strength: 75; 50; 70; 60; 57 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: Cetaphil Daily Facial Moisturizer with suncreen SPF 50
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OCTINOXATE	75 mg/mL
OCTISALATE	50 mg/mL
OCTOCRYLENE	70 mg/mL
OXYBENZONE	60 mg/mL
TITANIUM DIOXIDE	57 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
4Y5P7MUD51	Internal UNII lookup
4X49Y0596W	Internal UNII lookup
5A68WGF6WM	Internal UNII lookup
95OOS7VE0Y	Internal UNII lookup
15FIX9V2JP	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
6650d137-e69e-4ec2-8311-3de74bf21315	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0299-4930-02	Cetaphil Daily Facial Moisturizer with suncreen SPF 50	1 in 1 CARTON	LOTION	1		7
0299-4930-02	Cetaphil Daily Facial Moisturizer with suncreen SPF 50	50 mL in 1 TUBE	LOTION	50		7

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Octinoxate	ACTIVE INGREDIENT	4Y5P7MUD51	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Octisalate	ACTIVE INGREDIENT	4X49Y0596W	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Octocrylene	ACTIVE INGREDIENT	5A68WGF6WM	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Oxybenzone	ACTIVE INGREDIENT	95OOS7VE0Y	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Titanium Dioxide	ACTIVE INGREDIENT	15FIX9V2JP	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Octinoxate	ACTIVE MOIETY	4Y5P7MUD51	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Octisalate	ACTIVE MOIETY	4X49Y0596W	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Octocrylene	ACTIVE MOIETY	5A68WGF6WM	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Oxybenzone	ACTIVE MOIETY	95OOS7VE0Y	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Titanium Dioxide	ACTIVE MOIETY	15FIX9V2JP	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Aluminum Hydroxide	INACTIVE INGREDIENT	5QB0T2IUN0	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Cetyl Alcohol	INACTIVE INGREDIENT	936JST6JCN	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Chlorphenesin	INACTIVE INGREDIENT	I670DAL4SZ	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Dimethicone	INACTIVE INGREDIENT	92RU3N3Y1O	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Ethylparaben	INACTIVE INGREDIENT	14255EXE39	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Glycerin	INACTIVE INGREDIENT	PDC6A3C0OX	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Methylparaben	INACTIVE INGREDIENT	A2I8C7HI9T	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
PEG-100 Stearate	INACTIVE INGREDIENT	YD01N1999R	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Phenoxyethanol	INACTIVE INGREDIENT	HIE492ZZ3T	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Potassium Cetyl Phosphate	INACTIVE INGREDIENT	03KCY6P7UT	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Propylene Glycol	INACTIVE INGREDIENT	6DC9Q167V3	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Stearic Acid	INACTIVE INGREDIENT	4ELV7Z65AP	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Tocopherol	INACTIVE INGREDIENT	R0ZB2556P8	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Water	INACTIVE INGREDIENT	059QF0KO0R	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1
Xanthan Gum	INACTIVE INGREDIENT	TTV12P4NEE	CETAPHIL DAILY FACIAL MOISTURIZER SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0299-4930	CETAPHIL DAILY FACIAL MOISTURIZER WITH SUNCREEN SPF 50 (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [GALDERMA LABORATORIES, L.P.]	7	Current NDC, Legacy NDC, 2 package rows	20240420_6650d137-e69e-4ec2-8311-3de74bf21315.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 12 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sun Juice Body Mist Sunscreen SPF30 - Cotton Candy Skies PARADISO	AVOBENZONE, HOMOSALATE, OCTISALATE	Koco Life LLC	568083ff-0da9-7f14-e063-6394a90a4301	2026-07-13	Warnings	Exact identifier application number: M020
Sun Juice Body Mist Sunscreen SPF30 - Vanilla Breeze PARADISO	AVOBENZONE, HOMOSALATE, OCTISALATE	Koco Life LLC	3cc62c97-70c5-17f7-e063-6394a90abe25	2026-07-13	Warnings	Exact identifier application number: M020
Norwex Lip Glaze Broad Spectrum SPF 30 Rose	ZINC OXIDE	Norwex Usa, Inc.	565feded-8e25-e628-e063-6294a90aee48	2026-07-11	Warnings	Exact identifier application number: M020
PoutScreen Lip Treatment Lemon Meringue	AVOBENZONE, OCTINOXATE, OCTOCRYLENE	NAKED SUNDAYS PTY LTD	563e3ab9-4ee2-279c-e063-6294a90a7cf1	2026-07-10	Warnings	Exact identifier application number: M020
INN BEAUTY SUN BALM SPF30 BROAD SPECTRUM LIP BALM - ROSY BROWN	ZINC OXIDE	COSMAX USA, CORPORATION	5643a73d-757c-702d-e063-6294a90a2c12	2026-07-10	Warnings	Exact identifier application number: M020
INN BEAUTY SUN BALM SPF30 BROAD SPECTRUM LIP BALM - LATTE	ZINC OXIDE	COSMAX USA, CORPORATION	5643d655-e335-5643-e063-6394a90a483a	2026-07-10	Warnings	Exact identifier application number: M020
MUSELY DAYCREAM SPF40	ZINC OXIDE	COSMAX USA, CORPORATION	56443156-3edb-a643-e063-6394a90adf9f	2026-07-10	Warnings	Exact identifier application number: M020
Hello Sun Silky Glow Broad Spectrum SPF40	ZINC OXIDE	Cosmax USA, Corporation	56445f2d-8e5a-34eb-e063-6294a90ae26e	2026-07-10	Warnings	Exact identifier application number: M020
Hello Kitty Fun Broad Spectrum SPF 40	ZINC OXIDE	Cosmax USA Corporation	5644854e-18d6-617d-e063-6294a90ab3e7	2026-07-10	Warnings	Exact identifier application number: M020
VERSED DAILY SUNSCREEN SPF 50	HOMOSALATE, OCTISALATE, AVOBENZONE	COSMAX USA, CORP	5644ca1e-9032-d3fb-e063-6394a90a961e	2026-07-10	Warnings	Exact identifier application number: M020
Hello Kitty Sunny Days Broad Spectrum SPF 40	ZINC OXIDE	Cosmax USA Corporation	5644855d-f864-e07b-e063-6394a90a5148	2026-07-10	Warnings	Exact identifier application number: M020
VERSED MULTI SERUM SKIN TINT SPF 40	ZINC OXIDE	COSMAX USA, CORP	5644d49f-08b9-e806-e063-6294a90a80f9	2026-07-10	Warnings	Exact identifier application number: M020
VERSED MULTI SERUM SKIN TINT SPF 40 LIGHT NEUTRAL	ZINC OXIDE	COSMAX USA, CORP	564682e5-1051-9936-e063-6394a90abe1d	2026-07-10	Warnings	Exact identifier application number: M020
VERSED MULTI SERUM SKIN TINT SPF 40 LIGHT WRM	ZINC OXIDE	COSMAX USA, CORP	5646e069-5461-12c5-e063-6294a90abacb	2026-07-10	Warnings	Exact identifier application number: M020
Protect Sport Sunscreen	BROAD SPECTRUM SPF 30	Opal Day Spa	564704f2-b26a-d737-e063-6294a90aa6ff	2026-07-10	Warnings	Exact identifier application number: M020
VERSED MULTI SERUM SKIN TINT SPF 40 LIGHT MEDIUM NEUTRAL	ZINC OXIDE	COSMAX USA, CORP	5647162a-610e-2789-e063-6294a90a7549	2026-07-10	Warnings	Exact identifier application number: M020
VERSED MULTI SERUM SKIN TINT SPF 40 LIGHT MEDIUM OLIVE	ZINC OXIDE	COSMAX USA, CORP	56472adb-572d-5a52-e063-6294a90a3cc3	2026-07-10	Warnings	Exact identifier application number: M020
VERSED MULTI SERUM SKIN TINT SPF 40 MEDIUM COOL	ZINC OXIDE	COSMAX USA, CORP	56474782-beff-8437-e063-6294a90a8322	2026-07-10	Warnings	Exact identifier application number: M020
VERSED MULTI SERUM SKIN TINT SPF 40 MEDIUM PEACH	ZINC OXIDE	COSMAX USA, CORP	564749f3-e820-9003-e063-6294a90a0265	2026-07-10	Warnings	Exact identifier application number: M020
VERSED MULTI SERUM SKIN TINT SPF 40 TAN NEUTRAL	ZINC OXIDE	COSMAX USA, CORP	56477f58-3878-81fa-e063-6294a90a87b7	2026-07-10	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4Y5P7MUD51	OCTINOXATE	83834-59-7	OCTINOXATE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
5A68WGF6WM	OCTOCRYLENE	6197-30-4	OCTOCRYLENE
95OOS7VE0Y	OXYBENZONE	131-57-7	OXYBENZONE
15FIX9V2JP	TITANIUM DIOXIDE	13463-67-7	TITANIUM DIOXIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0299-4930-02	00299493002	1 TUBE in 1 CARTON (0299-4930-02) / 50 mL in 1 TUBE	1 tube	2012-01-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Cetaphil Daily Facial Moisturizer with suncreen SPF 50+	Galderma Laboratories, L.P. \| G Production Inc.	2024-04-17	HUMAN OTC DRUG LABEL	7
NuCaraRXPAK - NuCare Pharmaceuticals,Inc.	NuCare Pharmaceuticals,Inc.	2021-07-28	HUMAN PRESCRIPTION DRUG LABEL	3
NuCaraClinPAK - NuCare Pharmaceuticals,Inc.	NuCare Pharmaceuticals,Inc.	2021-05-04	HUMAN PRESCRIPTION DRUG LABEL	2