Blue Ice Topical Analgesic Gel

Manufacturer
International Wholesale | Jell Pharmaceuticals Pvt Ltd. | Jell Pharmaceuticals Pvt Ltd
Effective date
2025-07-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:06:46

Label at a glance#

ProductBlue Ice Topical Analgesic Gel
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL
Label structure11 sections

Indications and uses

for temporary relief of minor aches and pains in muscles and joints associated with: simple backaches, strains sprains sports injuries arthritis bruises

Dosage and administration

clean affected area before applying product adults and children 2 years of age and older; apply to affected area not more than 3 to 4 times daily

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 1.0%
Camphor 0.5%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses:

INDICATIONS & USAGE SECTION

  • for temporary relief of minor aches and pains in muscles and joints associated with:
  • simple backaches,
  • strains
  • sprains
  • sports injuries
  • arthritis
  • bruises

Warnings

WARNINGS SECTION

FOR EXTERNAL USE ONLY

Do not use:

  • with other topical pain relievers
  • with heating pads or heating devices

When using this product

OTC - WHEN USING SECTION

  • do not use in or near eyes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days
  • redness or irritation develops

If pregnant or breastfeeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use

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

  • clean affected area before applying product
  • adults and children 2 years of age and older; apply to affected area not more than 3 to 4 times daily

Inactive Ingredients

INACTIVE INGREDIENT SECTION

ammonium hydroxide, carbomer, cupric sulfate, FD&C Blue No. 1, isopropyl alcohol, magnesium sulfate, sodium hydroxide, thymol, water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1043046camphor 0.5 % / menthol 1 % Topical GelPSN1
1043046camphor 0.005 MG/MG / menthol 0.01 MG/MG Topical GelSCD1
1043046camphor 0.5 % / menthol 1 % Topical GelSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52862-901-01Blue Ice Topical Analgesic Gel227 g in 1 TUBEGEL2271

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52862-90152862-901-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
Blue Ice Topical Analgesic GelICE GELInternational Wholesale397cd306-078d-5b7d-e063-6294a90a8bbc2025-07-03WarningsExact identifier
ndc (package): 52862-901-01
ndc (product): 52862-901
ndc11 (package): 52862090101
spl id: 397ce4f6-f5af-18f1-e063-6394a90ad7c5
spl set id: 397cd306-078d-5b7d-e063-6294a90a8bbc

Reported adverse events (FAERS/openFDA)#

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