FDA.reportPublic FDA data

GZE Rice Raw PulpShampoo

Manufacturer
Guangzhou Yilong Cosmetics Co.,Ltd.
Effective date
2024-06-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:01:00

Label at a glance#

ProductGZE Rice Raw PulpShampoo
Active ingredientORYZA SATIVA WHOLE, LAURAMIDOPROPYL BETAINE, AMINO ACIDS, RICE, COCAMIDOPROPYL BETAINE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ORYZA SATIVA WHOLE 5%
COCAMIDOPROPYL BETAINE 5%
AMINO ACIDS, RICE 38.7%
LAURAMIDOPROPYL BETAINE 5%

OTC - PURPOSE SECTION

Our GZE rice raw pulp shampoo is packed with vital nutrients that may reduce hairdamage,and help infuse your hair with nutrients, lock in moisture and hydrate the scalp and hair,leaving your hair well-hydrated and supple.

INDICATIONS & USAGE SECTION


After wet hair, apply proper amount of rice raw pulp shampoo on the palm, rub it into foam,smear it on the wet hair and gently
massage.Rinse thoroughly.

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

After wet hair, apply proper amount of rice raw pulp shampoo on the palm, rub it into foam, smear it on the wet hair and gently massage.Rinse thoroughly.

INACTIVE INGREDIENT SECTION

HISTIDINE
SODIUM CITRATE
PANTHENYL ETHYL ETHER
WATER
PANTHENOL
POLYQUATERNIUM-10 (1000 MPA.S AT 2%)
SODIUM LAUROYL SARCOSINATE
FRAGRANCE 13576
HISTIDINE
TETRASODIUM EDETATE DIHYDRATE
ANHYDROUS CITRIC ACID
SODIUM COCOYL ISETHIONATE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-11483566-114-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
HISTIDINE4QD397987EIACT
SODIUM CITRATE1Q73Q2JULRIACT
PANTHENYL ETHYL ETHERF4WMF8NX3BIACT
WATER059QF0KO0RIACT
PANTHENOLWV9CM0O67ZIACT
POLYQUATERNIUM-10 (1000 MPA.S AT 2%)GMR4PEN8PKIACT
ORYZA SATIVA WHOLE84IVV0906ZACTIB
LAURAMIDOPROPYL BETAINE23D6XVI233ACTIB
SODIUM LAUROYL SARCOSINATE632GS99618IACT
FRAGRANCE 135765EM498GW35IACT
TETRASODIUM EDETATE DIHYDRATE3JGX4KKZ4AIACT
AMINO ACIDS, RICE5ET1T25H82ACTIB
COCAMIDOPROPYL BETAINE5OCF3O11KXACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
SODIUM COCOYL ISETHIONATE518XTE8493IACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
269c4795-5ce2-1534-e063-6394a90a485d18df3f4d-0abb-0aa1-e063-6394a90a2f252024-11-10WarningsExact identifier
spl set id: 18df3f4d-0abb-0aa1-e063-6394a90a2f25

Reported adverse events (FAERS/openFDA)#

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