Active Ingredients
Menthol 1.0%
Camphor 0.5%
Lucky Blue Ice
FDA Label NDC 47046-167
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Anicare Pharmaceuticals Pvt. Ltd. for the product Lucky Blue Ice (NDC 47046-167). 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 active ingredients, purpose, use, warnings, keep out of reach of children, directions, inactive ingredients, package label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Topical Analgesic
Use
Lucky Super Soft Blue Ice Gel to provide temporary relief of minor pains and aches in your body's joints and muscles associated with:
- sports injuries
- sprains
- arthritis
- bruises
Warnings
for external use only
Do not apply to wound or damaged skin. Do not bandage the applied surface.
If condition worsens, discontinue use of this product.
Consult a physician if symptoms persist for more than 7 days.
Avoid contact with mucus membranes and eyes.
Do not use with heating devices or pads.
Keep Out Of Reach Of Children
If pregnant or breast-feeding, ask a health professional before use
Directions
Apply liberally to painful zones and massage until absorbed into the skin. Repeat daily 3 or 4 times. Keep out of reach of children. Do not apply to children below two years of age.
Inactive Ingredients
Deionized Water, Isopropyl Alcohol, Propylene Glycol,Carbopol, PEG-40 Hydrogenated Castor Oil, Sodium Hydroxide,
Disodium EDTA, Benzyl Alcohol, BHT, FDC Blue No. 1
Package Label
Package Label (Packagelabel)
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