DO ME DELAY- lidocaine hcl cream

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Lidocaine HCL 4%

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.

SPL UNCLASSIFIED SECTION

Do not use if seal is broken.

Inactive Ingredients

Cyclopentasiloxane, Emu Oil, Ethoxydiglycol, Ethylhexylglycerin, Glycerin, Isopropyl Myristate, Phenoxyethanol, Polyacrylate Crosspolymer-6, Polysorbate 60, Water, Xanthan Gum

SPL UNCLASSIFIED SECTION

Questions? 866-488-0066

Product Label & Box

INGREDIENTS AND APPEARANCE

DO ME DELAY 
lidocaine hcl cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70171-0051
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
CYCLOMETHICONE (UNII: NMQ347994Z)
POLYSORBATE 60 (UNII: CAL22UVI4M)
EMU OIL (UNII: 344821WD61)
ETHOXYDIGLYCOL (UNII: A1A1I8X02B)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYACRYLATE CROSSPOLYMER-6 (UNII: Q7UI015FF9)
WATER (UNII: 059QF0KO0R)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70171-0051-1	1 in 1 CARTON	05/01/2026
1		28 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	05/01/2026

Labeler - Prodigy Media Inc (080011622)