Label: DZUL - LIDO CREME- lidocaine hcl, menthol lotion
- NDC Code(s): 83037-041-02
- Packager: Caball Sales, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 25, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- USES:
- WARNINGS
-
WHEN USING
Use only as directed.
Avoid contact with eyes and mucous membranes.
Do not bandage tightly or use with a heating pad.
A transient burning sensation or redness may occur upon application but generally disappears in several days.Do not apply on large areas of the body or on damaged, broken, or irritated skin.
- STOP USE AND ASK A DOCTOR IF:
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS:
- OTHER SAFETY INFORMATION
-
INACTIVE INGREDIENT
Water, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Isopropyl Myristate, Glycol Stearate, Stearyl Alcohol, Glyceryl Stearate, PEG-100 Stearate, Sodium Lauryl Sulfate, Dimethicone, Glycerin, Caprylhydroxamic Acid, Caprylyl Glycol, Eucalyptus Globulus Leaf Oil, Phenoxyethanol, Methylpropanediol, Acrylamide/Sodium Acrylate Copolymer, Paraffinum Liquidum, Trideceth-6, Methylsulfonylmethane, Aloe Barbadensis (Aloe Vera) Leaf Juice, Rosmarinus Officinalis (Rosemary) Oil, Tocopheryl Acetate, Arnica Montana Flower Extract, Salix Alba Bark Extract, Glucosamine Sulfate, Chamomilla Recutita (Matricaria) Flower Extract, Capsicum Annuum Fruit Extract.
- DZUL - LIDO CREME ROLL-ON
-
INGREDIENTS AND APPEARANCE
DZUL - LIDO CREME
lidocaine hcl, menthol lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83037-041 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 1 g in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 4 g in 100 g Inactive Ingredients Ingredient Name Strength ALMOND OIL (UNII: 66YXD4DKO9) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) METHYLPROPANEDIOL (UNII: N8F53B3R4R) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) PEG-100 STEARATE (UNII: YD01N1999R) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) GLYCOL STEARATE (UNII: 0324G66D0E) SODIUM LAURYL SULFATE (UNII: 368GB5141J) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE 1000 (UNII: MCU2324216) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PHENOXYETHANOL (UNII: HIE492ZZ3T) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) ROSEMARY OIL (UNII: 8LGU7VM393) CHAMOMILE (UNII: FGL3685T2X) SALIX ALBA BARK (UNII: 205MXS71H7) CAPSICUM ANNUUM WHOLE (UNII: 7FKZ3QQQ1F) XANTHAN GUM (UNII: TTV12P4NEE) POLYSORBATE 20 (UNII: 7T1F30V5YH) GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83037-041-02 71 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 10/02/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 10/17/2022 Labeler - Caball Sales, Inc. (047422138)