7th MANNA PAIN RELIEF DROPS

MENTHOL, CAMPHOR (SYNTHETIC) TOPICAL HUMAN OTC DRUG

7th MANNA PAIN RELIEF DROPS is an FDA drug label for the active ingredient MENTHOL, CAMPHOR (SYNTHETIC) manufactured by 7TH MANNA (USA) PTE. LTD. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231111.

Generic name
MENTHOL, CAMPHOR (SYNTHETIC)
Manufacturer
7TH MANNA (USA) PTE. LTD.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
71856-423
Application
M017B
Label effective
20231111

About this product

7th MANNA PAIN RELIEF DROPS is an FDA-registered drug product whose active ingredient is MENTHOL, CAMPHOR (SYNTHETIC). It is labelled by 7TH MANNA (USA) PTE. LTD. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 71856-423, application M017B, label effective 20231111. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing MENTHOL, CAMPHOR (SYNTHETIC) are most often described in connection with: temporary relief, minor aches, pains muscles, joints associated, arthritis sprains, strains bruises, simple backaches. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredients Menthol 10% Camphor 3% Purpose Topical Analgesic

Indications & Usage

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

Dosage & Administration

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

Warnings

Warnings 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 avoid contact with the eyes do not apply to wounds or damaged skin do not bandage tightly Stop use and ask a doctor if 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, ask a healthcare provider before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Frequently asked questions

What is 7th MANNA PAIN RELIEF DROPS used for?
Uses For the temporary relief of minor aches and pains of muscles and joints associated with: arthritis sprains strains bruises simple backaches

Who makes 7th MANNA PAIN RELIEF DROPS?
7TH MANNA (USA) PTE. LTD. is the labeler of record for 7th MANNA PAIN RELIEF DROPS.

What form does 7th MANNA PAIN RELIEF DROPS come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is 7th MANNA PAIN RELIEF DROPS prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has 7th MANNA PAIN RELIEF DROPS been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.