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 01:51:33

Label at a glance#

Productpalm party
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

To help reduce bacteria on the skin. ​Recommended for repeated use.

Dosage and administration

Spray an adequate amount into your palm to fully coat your hands. Rub your hands together thoroughly 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

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • To help reduce bacteria on the skin.
  • ​Recommended for repeated use.

Warnings

WARNINGS SECTION

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

When using this product

OTC - WHEN USING SECTION

Do not use in or near 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

  • Spray an adequate amount into your palm to fully coat your hands.
  • Rub your hands together thoroughly until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

OTHER SAFETY INFORMATION

  • Store at 20℃ to 25℃ (68℉ to 77℉).
  • May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER, FRAGRANCE, ACID RED 18

Questions or comments?

OTC - QUESTIONS SECTION

213-396-1046 / MalachiPerez291@gmail.com

Box Front Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

IN MY GLAM GIRL ERA


PEACH MATCHA
HAND SANITIZER
Product PackagingProduct Packaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1367692ethanol 60 % Topical SprayPSN2
1367692ethanol 0.6 ML/ML Topical SpraySCD2
1367692ethanol 60 % Topical SpraySY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87322-1169-1palm party15 mL in 1 BOXSPRAY152
87322-1169-2palm party35 mL in 1 BOXSPRAY352
87322-1169-3palm party42 mL in 1 BOXSPRAY422
87322-1169-4palm party100 mL in 1 BOXSPRAY1002

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87322-116987322-1169-1, 87322-1169-2, 87322-1169-3, 87322-1169-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-01-15monthly-update2026-06-03 17:52:56

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 HAND SANITIZERDongyang Loulee Cosmetics Co.,Ltd.48786094-aa70-d0ca-e063-6394a90acd882026-03-25WarningsExact identifier
ndc (package): 87322-1169-4
ndc (package): 87322-1169-3
ndc (package): 87322-1169-1
ndc (package): 87322-1169-2
ndc (product): 87322-1169
ndc11 (package): 87322116903
ndc11 (package): 87322116904
ndc11 (package): 87322116901
ndc11 (package): 87322116902
spl id: 4de4c0c5-06cb-bc00-e063-6394a90a599e
spl set id: 48786094-aa70-d0ca-e063-6394a90acd88

Reported adverse events (FAERS/openFDA)#

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