FDA.reportPublic FDA data

ALLG ® Essentials Warm-up Accelerator Cream

Manufacturer
Global Products Group, LLC
Effective date
2022-01-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:47:33

Label at a glance#

ProductALLG Essentials Warm-up Accelerator
Active ingredientCamphor (Synthetic)
Label structure10 sections

Indications and uses

minor arthritis pain simple backache muscle sprains bruises muscle strains cramps

Dosage and administration

cleanse, rinse and dry skin prior to application apply generously to painful muscles and joints, gently massaging until the ALLG ® Warm-up Accelerator Cream disappears. repeat as necessary but no more than four times a day for optimum benefit, use daily for at least two weeks.

Storage and handling

store at room temperature with the cap closed Notice: because this product contains natural nutrients, color may vary

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 5%

Purpose

OTC - PURPOSE SECTION

Counterirritant

Uses

INDICATIONS & USAGE SECTION

  • minor arthritis pain
  • simple backache
  • muscle sprains
  • bruises
  • muscle strains
  • cramps

Warnings

WARNINGS SECTION

For external use only

Do not use if

OTC - DO NOT USE SECTION

  • skin is irritated or damaged
  • excessive irritation develops
  • 12 years of age or under

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes and mucous membranes
  • do not apply to wounds, damaged, broken or irritated skin
  • do not bandage tightly or use a heating pad
  • do not swallow. If swallowed, contact a physician or contact a poison control center immediately.

Stop use and ask doctor if

OTC - STOP USE SECTION

  • condition worses
  • symptoms persist for more than 7 days or clear up and occur again within a few days
  • redness develops

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

  • cleanse, rinse and dry skin prior to application
  • apply generously to painful muscles and joints, gently massaging until the ALLG ® Warm-up Accelerator Cream disappears.
  • repeat as necessary but no more than four times a day
  • for optimum benefit, use daily for at least two weeks.

Other

STORAGE AND HANDLING SECTION

  • store at room temperature with the cap closed
  • Notice: because this product contains natural nutrients, color may vary

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Acrylate/C10-30 Alkyl Acrylate Crosspolymer, Aescin (Horse Chestnut Extract), Aloe Vera, Arnica Montana Extract, C12-15 Alkyl Benzoate, Calcium Fructoborate, Chondroitin Sulfate, Diazolidinyl Urea, Dimethicone, Disodium EDTA, dl Panthenol, Glucosamine Sulfate, Glycerin, Glycerol Stearate, Hemp Oil, Hydroxypropyl methylcellulose, Iodopropynyl Butylcarbamate, Methyl Gluceth-20, Methyl Glucose Sesquistearate, Peppermint Oil, Polysorbate 20, Potassium Carbomer, Purified Water, Shea Butter, Tocopheryl Acetate, Trolamine Salicylate

Questions or comments?

OTC - QUESTIONS SECTION

Call (877) 383-2334

PRINCIPAL DISPLAY PANEL - 114 g Jar Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

• MADE WITH
HEMP
OIL
ORGANIC •

ALLG®
ESSENTIALS

WARM-UP
ACCELERATOR CREAM

GOOD FOR
YOGA
RUNNING
CROSS FIT
PILATIES
BOOT CAMPS

NET WT 4 OZ. (114g)

PRINCIPAL DISPLAY PANEL - 114 g Jar Label
PRINCIPAL DISPLAY PANEL - 114 g Jar Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
09b728d3-9521-67a6-95fe-30969d1d5187Product name520240828
5f07db61-095c-acca-e8e9-d0916b4c1947Product name220200616
98f556da-44be-c658-496e-47884da4e67bProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72593-154-142024-01-30C16284748780-11030e365-08c1-111a-e063-dadaa90a10e2ALLG ® Essentials Warm-up Accelerator Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72593-154-14ALLG Essentials Warm-up Accelerator114 g in 1 JARCREAM1142

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72593-154ALLG ESSENTIALS WARM-UP ACCELERATOR (CAMPHOR (SYNTHETIC)) CREAM [GLOBAL PRODUCTS GROUP, LLC]2Legacy NDC, 1 package rows20220126_16123f22-7197-4913-8017-aa80e6f47cd9.zip

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72593-15472593-154-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Name, UNII, Kind table
NameUNIIKind
Camphor (Synthetic)5TJD82A1ETACTIB
Methyl Glucose SesquistearateV1YW10H14DIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
Alkyl (C12-15) BenzoateA9EJ3J61HQIACT
ALOE VERA LEAFZY81Z83H0XIACT
ARNICA MONTANA WHOLEO80TY208ZWIACT
CALCITRIOLFXC9231JVHIACT
CHONDROITIN SULFATE (SHARK)2ZAJ1K50XHIACT
Diazolidinyl UreaH5RIZ3MPW4IACT
Iodopropynyl Butylcarbamate603P14DHEBIACT
Dimethicone92RU3N3Y1OIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
PANTHENOLWV9CM0O67ZIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
EscinRUU8G67GQMIACT
GLUCOSAMINE SULFATE POTASSIUM CHLORIDE15VQ11I66NIACT
GlycerinPDC6A3C0OXIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
Methyl Gluceth-20J3QD0LD11PIACT
Peppermint OilAV092KU4JHIACT
Potassium HydroxideWZH3C48M4TIACT
WATER059QF0KO0RIACT
Shea ButterK49155WL9YIACT
Sorbitan Monolaurate6W9PS8B71JIACT
Trolamine SalicylateH8O4040BHDIACT
Cannabis Sativa Seed Oil69VJ1LPN1SIACT

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
223bea3d-47ea-4c6f-8e28-454fec29981f16123f22-7197-4913-8017-aa80e6f47cd92022-01-24WarningsExact identifier
spl id: 223bea3d-47ea-4c6f-8e28-454fec29981f
spl set id: 16123f22-7197-4913-8017-aa80e6f47cd9

Reported adverse events (FAERS/openFDA)#

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