Drug Facts

Active Ingredient

Lidocaine HCl 4.00%

Purpose

Topical Analgesic

Uses

For the temporary relief of pain

Warnings

For external use only.
Avoid contact with eyes.
If symptoms persist for more than seven days, discontinue use and consult physician.

Keep out of reach of children.

If swallowed, consult physician.

Do not use

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

If pregnant or breast feeding,

contact physician prior to use.

Directions

Adults and children two-years of age or older:

Apply to affected area not more than three to four times daily.
Children under two-years of age: consult a physician.

Additional Information

Store at room temperature.

Other Ingredients

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aesculus Hippocastanum (Horse Chestnut) Extract, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Beta Alanine, Betaglucan, Boswellia Serrata Extract, Butyrospermum Parkii (Shea) Butter, Cannabis Sativa (Hemp) Seed Oil, Cetyl Esters, Dimethicone, Ethoxydiglycol, Ethylhexylglycerin, Ethyl Vanillin, Eucalyptus Globulus Oil, Glucosamine Sulfate, Glycerin, Glyceryl Stearate, Helianthus Annuus (Sunflower) Oil, l-Arginine, l-Carnitine, l-Citruline, Magnesium Sulfate, Methyl Gluceth-20, Methylsulfonylmethane (MSM), PEG-100 Stearate, Phenoxyethanol, Ribes Nigrum (Black Currant) Oil, Salix Alba (Willow) Bark Extract, Steareth-20, Triethanolamine.

Package Labeling:

Label

SUGAR BRANDS RESCUE PAIN RELIEF AND RECOVERY
lidocaine hydrochloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:73313-075
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	40 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
HORSE CHESTNUT (UNII: 3C18L6RJAZ)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
.BETA.-ALANINE (UNII: 11P2JDE17B)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
SHEA BUTTER (UNII: K49155WL9Y)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
CETYL ESTERS WAX (UNII: D072FFP9GU)
DIMETHICONE (UNII: 92RU3N3Y1O)
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ETHYL VANILLIN (UNII: YC9ST449YJ)
EUCALYPTUS OIL (UNII: 2R04ONI662)
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
ARGININE (UNII: 94ZLA3W45F)
LEVOCARNITINE (UNII: 0G389FZZ9M)
CITRULLINE (UNII: 29VT07BGDA)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
PEG-100 STEARATE (UNII: YD01N1999R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BLACK CURRANT (UNII: 9755T40D11)
SALIX ALBA BARK (UNII: 205MXS71H7)
STEARETH-20 (UNII: L0Q8IK9E08)
TROLAMINE (UNII: 9O3K93S3TK)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:73313-075-04	118 mL in 1 TUBE; Type 0: Not a Combination Product	08/20/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M017	08/20/2019

Labeler - Sugar Brands, LLC (050377177)

SUGAR BRANDS: Rescue Pain Relief & Recovery Cream