Easment advanced absorption cream

Manufacturer
Easment LLC
Effective date
2026-01-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:46:05

Label at a glance#

ProductEasment advanced absorption cream
Active ingredientCAPSAICIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Capsaicin 0.1%

OTC - PURPOSE SECTION

Topical Analgesic

DOSAGE & ADMINISTRATION SECTION

For the temporary relief of aches and pains of muscles and joints associated with: arthritis, simple backache, strains, sprains, bruises

WARNINGS SECTION

For external use only. Do not apply to wounds or damaged skin.

OTC - WHEN USING SECTION

You may experience a warm or slight burning sensation; this is normal and generally decreases with continued use. avoid contact with eyes and mucous membranes.do not bandage tightly.test on asmall area before first use .wash hands thoroughly after application

OTC - ASK DOCTOR SECTION

  • condition worsens
  • symptoms persist for more than 7 days or clear up andoccur again within a few days
  • severe burning, redness or irritation develops blistering or signs of skin injury occur

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • If swallowed, get medical help or contact a Poison Control Center right away.
  • If pregnant or breast-feeding,ask a doctor before use.

INDICATIONS & USAGE SECTION

  • Adults and children over 18 years:- apply to affected area - massage into painful area until fully absorbed - repeat as needed up to3-4 times daily
  • Children 18 years and under: ask a doctor
  • Wash hands with soap and water after applying

OTHER SAFETY INFORMATION

Store at room temperature 15-30C(59-86F).Keep tightly closed and avoid direct sunlight.Use consistently for best results

INACTIVE INGREDIENT SECTION

WATER、 CAPRYLIC/CAPRIC TRIGLYCERIDE、 BUTYLENE GLYCOl, BUTYROSPERMUM PARKII (SHEA) BUTTER、 CETEARYLALCOHOL, ALOEBARBADENSIS LEAF JUICE、 SODIUM ACRYLATES COPOLYMER, GLYCERYLSTEARATE、 NIACINAMIDE、 PEG-100 STEARATE、 PANTHENOL、 LECITHIN, ARNICA MONTANA FLOWER EXTRACT、CHAMOMILLA RECUTITA (MATRICARIA)FLOWER EXTRACT、 CAPRYLYL GLYCOL, ETHYLHEXYL GLYCERIN,CARBOMER, TOCOPHERYL ACETATE、 MENTHYL LACTATE、 AMINOMETHYL PROPANOL,SODIUM CITRATE, CHRYSANTHELLUM INDICUM EXTRACT

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

packagepackage

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
646333capsaicin 0.1 % Topical CreamPSN1
646333capsaicin 1 MG/ML Topical CreamSCD1
646333capsaicin 0.1 % Topical CreamSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codecapsaicinsupport.easmentllc.com/package.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87352-001-01Easment advanced absorption cream120 g in 1 CARTONCREAM1201

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87352-00187352-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

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
Easment advanced absorption creamCAPSAICIN 0.1%Easment LLC48de3ced-f67f-7c86-e063-6294a90a340c2026-01-20WarningsExact identifier
ndc (package): 87352-001-01
ndc (product): 87352-001
ndc11 (package): 87352000101
spl id: 48de3ced-f680-7c86-e063-6294a90a340c
spl set id: 48de3ced-f67f-7c86-e063-6294a90a340c

Reported adverse events (FAERS/openFDA)#

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