Body Sunscreen

Manufacturer: LYW BIOTECH CO LIMITED GUANGZHOU
Effective date: 2024-09-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:19:48

Label at a glance#

ProductBody Sunscreen

Active ingredientZINC OXIDE, TITANIUM DIOXIDE, AVOBENZONE

Label structure14 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

OTC - ASK DOCTOR SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - DO NOT USE SECTION

OTC - STOP USE SECTION

OTC - WHEN USING SECTION

WARNINGS SECTION

DOSAGE & ADMINISTRATION SECTION

INDICATIONS & USAGE SECTION

INSTRUCTIONS FOR USE SECTION

OTHER SAFETY INFORMATION

INACTIVE INGREDIENT SECTION

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7	Product name	1	20171122

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
81309-007-01	Body Sunscreen	120 mL in 1 TUBE	LOTION	120		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81309-007	BODY SUNSCREEN LOTION [LYW BIOTECH CO LIMITED GUANGZHOU]	1	1 package rows	20240921_22616f2c-eb71-8dd7-e063-6294a90ac318.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 20 matching rows.

Body Sunscreen
POLYHYDROXYSTEARIC ACID (2300 MW)
HYALURONATE SODIUM
ZINC OXIDE
PHENOXYETHANOL
DIMETHICONE
WATER
PANTHENOL
.ALPHA.-TOCOPHEROL ACETATE
LEVOMENOL
ETHYLHEXYLGLYCERIN
TITANIUM DIOXIDE
AVOBENZONE
BUTYLENE GLYCOL
CERAMIDE 3
ASCORBIC ACID
CERAMIDE 6 II, L-
SILICON DIOXIDE
CERAMIDE 1
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81309-007	81309-007-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
POLYHYDROXYSTEARIC ACID (2300 MW)	YXH47AOU0F	IACT
HYALURONATE SODIUM	YSE9PPT4TH	IACT
ZINC OXIDE	SOI2LOH54Z	ACTIB
PHENOXYETHANOL	HIE492ZZ3T	IACT
DIMETHICONE	92RU3N3Y1O	IACT
WATER	059QF0KO0R	IACT
PANTHENOL	WV9CM0O67Z	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
LEVOMENOL	24WE03BX2T	IACT
ETHYLHEXYLGLYCERIN	147D247K3P	IACT
TITANIUM DIOXIDE	15FIX9V2JP	ACTIB
AVOBENZONE	G63QQF2NOX	ACTIB
BUTYLENE GLYCOL	3XUS85K0RA	IACT
CERAMIDE 3	4370DF050B	IACT
ASCORBIC ACID	PQ6CK8PD0R	IACT
CERAMIDE 6 II, L-	717F57PF9J	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
CERAMIDE 1	5THT33P7X7	IACT
GLYCERIN	PDC6A3C0OX	IACT

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
22616f2c-eb72-8dd7-e063-6294a90ac318			22616f2c-eb71-8dd7-e063-6294a90ac318	2024-09-18	Warnings	Exact identifier spl id: 22616f2c-eb72-8dd7-e063-6294a90ac318 spl set id: 22616f2c-eb71-8dd7-e063-6294a90ac318

Reported adverse events (FAERS/openFDA)#

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