Ai Tape
FDA Label NDC 71590-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Active Intelligence, Llc for the product Ai Tape (NDC 71590-010). 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 drug facts, active ingredients, purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Menthol 7%
Camphor 3%
Purpose
Topical analgesic
Uses
temporary relief of minor aches and pains of muscles and joints associated with:
- simple backache • arthritis • muscle strains • sprains • bruises
Warnings
for external use only.
When using this product
- use only as directed. Read and follow all directions and warnings on this carton
- do not bandage tightly
- avoid contact with eyes and mucous membranes
- do not use at the same time as other topical analgesics
- condition worsens
- symptoms persist for more than 7 days or clear up and occur again within a few days
Stop use and ask a doctor if
If pregnant or breast feeding ask a health professional before use
Otc - Keep Out Of Reach Of Children
- if swallowed, get medical help or contact a Poison Control Center right away
Directions
adults and children over 12 years:
• apply one 10 inch strip to the affected area not more than 2 to 3 times daily
• each application can be worn not more than 4 day
children 12 years or younger:ask a doctor
Inactive Ingredients:
Methacrylic acid, Ethylhexylacrylate, Bentonite, Sodium stearate, Polypropylene Glycol.
Questions /Comments:
704-769-0166
Packaging
Ai Tape (Label 2)
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