Label: TYLENOL PRECISE PAIN RELIEVING LIDOCAINE 4%- lidocaine patch
- NDC Code(s): 69968-0927-2, 69968-0927-3, 69968-0927-4
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 30, 2025
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
-
Warnings
For external use only.
Do not use
- more than one patch at a time
- on wounds or damaged skin
- on raw surfaces or blistered areas
- with a heating pad
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Directions
adults and children 12 years of age and older:
children 12 to under 18 years of age, use with adult supervision
- apply contents of one pouch to affected area not more than 3 to 4 times daily
- remove a patch after at most 12 hours
- single-use patch. Do not reapply
- fold used patches so that the adhesive side sticks to itself and safely discard where children cannot get to them
children under 12 years of age: do not use
- Other Information
- Inactive Ingredients
- Questions or comments?
- SPL UNCLASSIFIED SECTION
-
PRINCIPAL DISPLAY PANEL - Tylenol Patch Label
NEW
TYLENOL ®
PRECISE TM
Pain Relieving Patch
Lidocaine 4% Topical Analgesic
Targeted penetrating pain relief
12
Stays on for
up to 12 hours
Designed with
specialized
adhesion
technology
Maximum
Strength
Lidocaine without
a prescription
4 INDIVIDUALLY SEALED PATCHES
3.3 in X 4.4 in (8.3 cm X 11.1 cm)
See back of carton for actual size
UNSCENTED
FOR EXTERNAL USE ONLY
-
INGREDIENTS AND APPEARANCE
TYLENOL PRECISE PAIN RELIEVING LIDOCAINE 4%
lidocaine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0927 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 40 mg Inactive Ingredients Ingredient Name Strength DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) ETHYLPARABEN (UNII: 14255EXE39) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL LAURATE (UNII: U0JQ94LABM) METHYLPARABEN (UNII: A2I8C7HI9T) POLYSORBATE 80 (UNII: 6OZP39ZG8H) POVIDONE (UNII: FZ989GH94E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0927-3 3 in 1 CARTON 10/06/2025 1 2 in 1 POUCH; Type 0: Not a Combination Product 2 NDC:69968-0927-2 2 in 1 CARTON 06/16/2025 2 1 in 1 POUCH; Type 0: Not a Combination Product 3 NDC:69968-0927-4 4 in 1 CARTON 06/16/2025 3 1 in 1 POUCH; 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 06/16/2025 Labeler - Kenvue Brands LLC (118772437)