Label: TOPCARE PAIN RELIEF MAXIMUM STRENGTH- lidocaine hydrochloride liquid
- NDC Code(s): 36800-529-25
- Packager: TOPCO ASSOCIATES
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 20, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
Do not use
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- on large areas of the body or on cut, irritated or swollen skin
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- on puncture wounds
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- for more than one week without consulting a doctor
When using this product
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- use only as directed. Read and follow all directions and warnings on this carton.
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- do not allow contact with the eyes
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- do not bandage or apply local heat (such as heating pads) to the area of use
- Directions
- Other Information
- Inactive ingredients
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PRINCIPAL DISPLAY PANEL
NDC# 36800-529-25
+TopCare health™
COMPARE TO THE ACTIVE INGREDIENT IN ASPERCREME® ODOR FREE WITH 4 % LIDOCAINE*
MAXIMUM STRENGTH
PAIN RELIEF Roll-On Liquid
Lidocaine HCl 4%
ODOR FREE
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- Temporary relief of pain
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- Helps pain-affected areas
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- No-touch applicator
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- Oil-Free
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- Paraben-Free
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- Alcohol-Free
With Aloe
NET WT 2.5 OZ (71 g)
CHILD-RESISTANT PACKAGING. CLOSE CAP TIGHTLY AFTER USE.
DISTRIBUTED BY
TOPCO ASSOCIATES LLC
ELK GROVE VILLAGE, IL 6007
© TOPCO RARA0819
QUESTIONS? 1-888-423-0139
*This product is not manufactured or distributed by Chattern, Inc., owner of the registered trademark Aspercreme® Odor Free with 4% Lidocaine.
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INGREDIENTS AND APPEARANCE
TOPCARE PAIN RELIEF MAXIMUM STRENGTH
lidocaine hydrochloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:36800-529 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 ALOE VERA LEAF (UNII: ZY81Z83H0X) CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) BENZYL ALCOHOL (UNII: LKG8494WBH) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36800-529-25 1 in 1 CARTON 04/12/2019 1 71 g in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M015 04/12/2019 Labeler - TOPCO ASSOCIATES (006935977)