LIDO E.R.CREME ROLL ON- lidocaine hcl cream

Lido E.R.CREME ROLL ON by

Drug Labeling and Warnings

Lido E.R.CREME ROLL ON by is a Otc medication manufactured, distributed, or labeled by Pharma-Natural. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

Active ingredient and Purpose

• Active ingredient: Purpose
• Lidocaine HCL 4%............................: Topical analgesic

Use

For the temporary relief of pain.

Warnings

For external use only. Avoid contact with the eyes.

Do not use

in large quantities, particularly over raw surfaces, or blistered areas.

Stop use and ask a doctor if

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

If pregnant or breast feeding,

ask a health professional before use.

Keep out of reach of children.

If swallowed, get medical help, or contact a Poison Control Center immediately.

Directions

▪adults 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: consult a doctor

Other information

▪ store in a cool dry place between (59-86°F)15-30°C

▪ don’t use if seal over cap is broken, torn, or missing

Inactive ingredients

caprylhydroxamic acid, caprylyl glycol, cyclomethicone 5, dimethicone, dimethyl sulfone, eucalyptus oil, glycerin, glyceryl monostearate, glycol stearate, methylpropanediol, PEG-100 stearate, PEG/PPG-18/18-dimethicone, phenoxyethanol, sodium lauryl sulfate, sodium polyacrylate, stearyl alcohol, sweet almond oil, trideceth-6, water

Questions or comments?

+1-888-469-3579 (M-F) 9 A.M. - 5 P.M. EST or www.advocatemeters.com

Distributed by:

Diabetic Supplu of Suncoast, Inc.

PO Box 2102, Vega Alta, PR 00692

Principal Display Panel

Lido E.R.

PAIN

RELIEVING

LIDOCAINE HCL 4%

Topical

Analgesic Cream

Maximum Strength

4 oz. (113 g)

INGREDIENTS AND APPEARANCE

LIDO E.R.CREME ROLL ON 
lidocaine hcl cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63788-115
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCOL STEARATE (UNII: 0324G66D0E)
METHYLPROPANEDIOL (UNII: N8F53B3R4R)
ALMOND OIL (UNII: 66YXD4DKO9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PEG-100 STEARATE (UNII: YD01N1999R)
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
WATER (UNII: 059QF0KO0R)
EUCALYPTUS OIL (UNII: 2R04ONI662)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63788-115-04	113 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	02/14/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	02/14/2020

Labeler - Pharma-Natural (138059287)