Otc - Active Ingredient
Lidocaine HCL 4%
Do Me Delay Cream
FDA Label NDC 70171-0051
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Prodigy Media Inc for the product Do Me Delay (NDC 70171-0051). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, keep out of reach of children, directions, other, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
External Analgesic
Indications & Usage
For the temporary relief of pain and itching associated with sunburns, minor cuts, insect bites, and skin irritations
Warnings
. For external use only.
. Avoid contact with eyes
Stop use and ask a doctor if
. Condition worsens or symptoms persist for more than 7 days
. Symploms clear up and occur again within a few days
. Do not use in large quantities, particulary over raw surfaces or blistered areas. Do not exceed the recommended daily dosage
unless directed by a doctor.
Do not use
. On wounds or damaged skin.
Keep Out Of Reach Of Children
If product is swallowed, get medical help or contact a Poison Control Center right away.
Directions
Adulls and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: do
not use, consult a physician.
Other
Do not use if seal is broken.
Questions? 866-488-0066
Inactive Ingredients
Cyclopentasiloxane, Emu Oil, Ethoxydiglycol, Ethylhexylglycerin, Glycerin, Isopropyl Myristate, Phenoxyethanol, Polyacrylate Crosspolymer-6, Polysorbate 60, Water, Xanthan Gum
Product Label & Box
Dm Box (Dm)
* Please review the disclaimer below.
