SUGAR BRANDS RESCUE PAIN RELIEF AND RECOVERY- lidocaine hydrochloride cream

SUGAR BRANDS Rescue Pain Relief and Recovery by

Drug Labeling and Warnings

SUGAR BRANDS Rescue Pain Relief and Recovery by is a Otc medication manufactured, distributed, or labeled by Sugar Brands, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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:

INGREDIENTS AND APPEARANCE

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

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

Inactive Ingredients
Ingredient Name	Strength
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)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	08/20/2019

Labeler - Sugar Brands, LLC (050377177)