FDA.reportPublic FDA data

7th MANNA PAIN RELIEF DROPS

Manufacturer
7TH MANNA (USA) PTE. LTD.
Effective date
2023-11-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:00:08

Label at a glance#

Product7th MANNA PAIN RELIEF DROPS
Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)
Label structure8 sections

Indications and uses

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

Dosage and administration

For adults: Apply to affected area no more than 3 to 4 times daily

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 10%

Camphor 3%

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:

  • arthritis
  • sprains
  • strains
  • bruises
  • simple backaches

Warnings

WARNINGS SECTION

For external use only.

Use only as directed.

Flammable

  • keep away from fire, flame, sparks and heated surfaces
  • tighten cap firmly

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

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

For adults: Apply to affected area no more than 3 to 4 times daily

Other Information

SPL UNCLASSIFIED SECTION

  • Store at room temperature
  • Do not use if printed safety seal on cap is broken or missing

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf (Aloe vera gel) Juice, Aqua (Deionized water), Arnica Montana Flower Extract, Calendula Officinalis Extract, Emu Oil, Dimethyl Sulfoxide (DMSO),Ethylhexylglycerin, HypericumPerforatum (St.John's Wort),Isopropyl Alcohol, Methyl Salicylate (Wintergreen) Oil, Olea Europaea (Olive) Oil, Phenoxyethanol, Polysorbate-20, SD-Alcohol 40B.

Questions?

OTC - QUESTIONS SECTION

Call us at 1-800-230-8055

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer PackageOuter Package

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1987413camphor 3 % / menthol 10 % Topical SolutionPSN2
1987413camphor 30 MG/ML / menthol 100 MG/ML Topical SolutionSCD2
1987413camphor 3 % / menthol 10 % Topical SolutionSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71856-423-007th MANNA PAIN RELIEF DROPS1 in 1 BOXLIQUID12
71856-423-007th MANNA PAIN RELIEF DROPS30 mL in 1 BOTTLELIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71856-4237TH MANNA PAIN RELIEF DROPS (MENTHOL, CAMPHOR (SYNTHETIC)) LIQUID [7TH MANNA (USA) PTE. LTD.]2Current NDC, 2 package rows20231112_699c668c-4f54-4f18-b585-bdcebe7a2c4e.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71856-42371856-423-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
GREEN OLIVE6HD2W46UEGIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYSORBATE 207T1F30V5YHIACT
MENTHOLL7T10EIP3AACTIB
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
EMU OIL344821WD61IACT
DIMETHYL SULFOXIDEYOW8V9698HIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
HYPERICUM PERFORATUM WHOLEXK4IUX8MNBIACT
ISOPROPYL ALCOHOLND2M416302IACT
METHYL SALICYLATELAV5U5022YIACT

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
7th MANNA PAIN RELIEF DROPSMENTHOL, CAMPHOR (SYNTHETIC)7TH MANNA (USA) PTE. LTD.699c668c-4f54-4f18-b585-bdcebe7a2c4e2023-11-11WarningsExact identifier
ndc (package): 71856-423-00
ndc (product): 71856-423
ndc11 (package): 71856042300
spl id: 09dc19d0-24b9-bd12-e063-6294a90ab40f
spl set id: 699c668c-4f54-4f18-b585-bdcebe7a2c4e

Reported adverse events (FAERS/openFDA)#

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