Kinkan Liniment
FDA Label NDC 51027-0007

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Kinkando Co., Ltd . for the product Kinkan (NDC 51027-0007). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding other, active ingredients, purpose, uses, warnings, do not use on, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Other

→ Active Ingredients

→ Purpose

→ Uses

→ Warnings

→ Do Not Use On

→ When Using This Product

→ Stop Use And Ask A Doctor If

→ Keep Out Of Reach Of Children.

→ Directions

→ Other Information

→ Inactive Ingredients

→ Questions And Comments

→ Principal Display Panel - 50 Ml Bottle Label

Other

Drug Facts

Active Ingredients

Ammonia 2.3%

Camphor 3.1%

Menthol 6.0%

Purpose

External Analgesic

Uses

Temporary relief of minor aches and pains of muscles and joints due to

simple backache
arthritic
strains
bruises
sprains

Warnings

For external use only

Flammable keep away from fire or flame

Do Not Use On

wounds
damaged skin

When Using This Product

avoid contact with the eyes and mouth
do not bandage tightly

Stop Use And Ask A Doctor If

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

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact. “a Poison Control Center right away.”

Directions

Adults and children 6 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 6 years of age: Do not use, consult a doctor.