FDA.reportPublic FDA data

N-LABS SOLAR MAX Topical Analgesic

Manufacturer
NUTRIOMO LABS PTE. LTD.
Effective date
2023-11-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:21:59

Label at a glance#

ProductN-LABS SOLAR MAX Topical Analgesic
Active ingredientMENTHOL, CAPSAICIN
Label structure8 sections

Indications and uses

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

Dosage and administration

● use only as directed ● shake well before each use ● with the roller facing down, roll ball against skin to apply a thin layer of product to affected area ● massage gently into skin ● wait 30 minutes before reapplying consult a doctor Adults and children 18 years of age and older: Children under 18 years of age:

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 8% Capsaicin 0.025%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with:

● simple backache ● arthritis ● strains ● bruises ● sprains

Warnings

WARNINGS SECTION

For external use only. Use only as directed.

Do not use

OTC - DO NOT USE SECTION

● on wounds, damaged, or irritated skin ● with a heating pad ● if you are allergic to capsicum or chili peppers

When using this product

OTC - WHEN USING SECTION

● avoid contact with the eyes or mucous membranes ● do not bandage tightly ● a transient burning sensation may occur upon application but generally disappears in several days ● do not expose the treated area to heat or direct sunlight ● do not have water contact on area of skin where product is applied as this may cause a “burning” sensation due to the active ingredients in the product

Stop use and ask a doctor if

OTC - STOP USE SECTION

● condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days ● redness is present or irritation develops ● a severe burning sensation occurs

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a healthcare provider 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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

● use only as directed ● shake well before each use ● with the roller facing down, roll ball against skin to apply a thin layer of product to affected area ● massage gently into skin ● wait 30 minutes before reapplying consult a doctor Adults and children 18 years of age and older: Children under 18 years of age:

Other Information

SPL UNCLASSIFIED SECTION

● Store at room temperature 20-25°C (68-77°F).  ● Do not use if printed safety seal on cap is broken or missing” to keep the consistency.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Angelica Archangelica Extract, Aqua (Deionized Water), Arnica Montana Flower Extract, Boswellia Serrata Extract, Calendula Officinalis Extract, Camellia Sinensis (Green Tea) Extract, Carbomer, Centella Asiatica (Gotu Kola) Extract, Chamomilla Matricaria (Chamomile) Extract, Ethylhexylglycerin, Eucalyptus Globulus Oil, Glycerin, llex Paraguariensis (Yerba Mate') Extract, Methylsulfonylmethane (MSM), Phenoxyethanol, Polysorbate-20, SD-Alcohol 40B, Sodium Lauryl Sulfate, Triethanolamine

Questions?

OTC - QUESTIONS SECTION

Call us at 1-800-856-5587

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label00Label00

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71856-27171856-271-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
INDIAN FRANKINCENSE4PW41QCO2MIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
CENTELLA ASIATICA TRITERPENOIDS4YS74Q4G4JIACT
CHAMOMILEFGL3685T2XIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
EUCALYPTUS OIL2R04ONI662IACT
GLYCERINPDC6A3C0OXIACT
ILEX PARAGUARIENSIS LEAF1Q953B4O4FIACT
DIMETHYL SULFONE9H4PO4Z4FTIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYSORBATE 207T1F30V5YHIACT
SODIUM LAURYL SULFATE368GB5141JIACT
TROLAMINE9O3K93S3TKIACT
MENTHOLL7T10EIP3AACTIB
CAPSAICINS07O44R1ZMACTIB

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
2bb7c6c9-8f28-cf81-e063-6294a90a7adb96b0c6cc-0ef6-4408-b879-9ff285759cbe2025-01-14WarningsExact identifier
spl set id: 96b0c6cc-0ef6-4408-b879-9ff285759cbe

Reported adverse events (FAERS/openFDA)#

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