palm party

Manufacturer
Dongyang Loulee Cosmetics Co.,Ltd. | Nanjing Ningjitong Pharmaceutical Biotechnology Co., Ltd
Effective date
2026-03-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:51:34

Label at a glance#

Productpalm party
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 60%

Purpose(s)

OTC - PURPOSE SECTION

Antisepti

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

  • Flammable. Keep away from fire or flame.
  • For external use only.

Do not use

OTC - DO NOT USE SECTION

In the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Irritation or rash appears and lasts.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER, FRAGRANCE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, ARGININE, PHENOXYETHANOL

Questions or comments?

OTC - QUESTIONS SECTION

213-396-1046 / MalachiPerez291@gmail.com

Box Front Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product PackagingProduct Packaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581658ethanol 60 % Topical GelPSN2
581658ethanol 0.6 ML/ML Topical GelSCD2
581658ethanol 60 % Topical GelSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87322-1614-1palm party30 mL in 1 CARTONGEL302
87322-1614-2palm party35 mL in 1 CARTONGEL352
87322-1614-3palm party42 mL in 1 CARTONGEL422
87322-1614-4palm party100 mL in 1 CARTONGEL1002

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87322-161487322-1614-1, 87322-1614-2, 87322-1614-3, 87322-1614-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-01-16monthly-update2026-06-03 17:52:53

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
palm partyALCOHOL GELDongyang Loulee Cosmetics Co.,Ltd.487c4724-b618-a071-e063-6394a90aa7822026-03-25WarningsExact identifier
ndc (package): 87322-1614-1
ndc (package): 87322-1614-4
ndc (package): 87322-1614-2
ndc (package): 87322-1614-3
ndc (product): 87322-1614
ndc11 (package): 87322161401
ndc11 (package): 87322161402
ndc11 (package): 87322161404
ndc11 (package): 87322161403
spl id: 4de4c2d0-3892-b947-e063-6394a90ab3b2
spl set id: 487c4724-b618-a071-e063-6394a90aa782

Reported adverse events (FAERS/openFDA)#

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