Label: TIDL PAIN RELIEF NUMBING TIDL- pain relief patch
- NDC Code(s): 79740-009-01, 79740-009-02
- Packager: The Anthos Group
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 21, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
Wamings
For extemal use only .
Do not use a on puncture wounds , cuts , imitated , damaged or swollen skin
more than 1 path on your body at a time or with other topical analgesics at the same time
with a heating pad or apply local heat to the area of use
When using his product
use only as directed
do not bandage tighty
avoid contact with eyes and mucous membranes
rare cases of serous bums have been reported with products of this type
a transient buming sensation may occur upon application but enerally disappears in several days
dispose of used patch in manner hat always keeps products away from children and pets . Used patches still contain e g po at can po s ad fs f a hid or pt chews or ingests this patch
Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days
symptoms ear up and occur again within a few days
severe burning sensation, redness or irritation develops
you experience signs of skin inur , such as pain , sw , or blistering where the product was appliedIf pregnant or breast-feeing , ask a health professional efore use . ep out of each of hilden .If swallowed , get medical help or contact a Poison Control Center night away - KEEP OUT OF REACH OF CHILDREN
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
TIDL PAIN RELIEF NUMBING TIDL
pain relief patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79740-009 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 3 g in 100 LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 4 g in 100 Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) METHYL SALICYLATE (UNII: LAV5U5022Y) ALCOHOL (UNII: 3K9958V90M) TARTARIC ACID (UNII: W4888I119H) DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K) CAPSICUM (UNII: 00UK7646FG) WATER (UNII: 059QF0KO0R) EDETIC ACID (UNII: 9G34HU7RV0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79740-009-01 5 in 1 BOX 08/31/2020 1 NDC:79740-009-02 1 in 1 BAG; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 08/31/2020 Labeler - The Anthos Group (117511051) Establishment Name Address ID/FEI Business Operations THE ANTHOS GROUP 117511051 manufacture(79740-009)
