Label: AIPATCH NUMBING PAIN RELIEF- lidocaine patch
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NDC Code(s):
71590-012-05,
71590-012-10,
71590-012-15,
71590-012-25, view more71590-012-30
- Packager: Active Intelligence, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 24, 2026
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Purpose
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Use
for the temporary relief of pain
Warnings
for external use only
When using this product
• use only as directed. Read and follow all directions and warnings on this carton
• do not bandage tightly
• avoid contact with eyes and mucous membranes
• do not use at the same time as other topical analgesics
• do not remove when wet or directly after shower, allow to dry and then slowly removeStop use and ask a doctor if
• condition worsens
• symptoms persist for more than 7 days or clear up and occur again within a few days
• you experience signs of skin injury, such as pain, swelling or blistering where the patch was applied• If pregnant or breast-feeding, ask a health professional before use
- Directions
- Inactive Ingredients
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SPL UNCLASSIFIED SECTION
Maximum Strength Lidocaine Patch Without a Prescription
QuadFlex Technology | Stays in place | Up to 12 hours of wear time
Made in USA
AIPATCH TM
For detailed usage instructions, scan the QR code or visit www.activeintell.com
Questions/Comments: (704) 769-0166
Manufactured and distributed by Active Intelligence,
LLC -A Nutriband, Inc company: 100 Sweetree St
Cherryville, NC 28021 - Packaging
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INGREDIENTS AND APPEARANCE
AIPATCH NUMBING PAIN RELIEF
lidocaine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71590-012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 40 mg in 1 g Inactive Ingredients Ingredient Name Strength ACRYLIC ACID (UNII: J94PBK7X8S) LINSEED OIL (UNII: 84XB4DV00W) POLYSORBATE 80 (UNII: 6OZP39ZG8H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71590-012-25 5 in 1 BOX 08/06/2025 1 5 in 1 POUCH 1 0.624 g in 1 PATCH; Type 0: Not a Combination Product 2 NDC:71590-012-15 3 in 1 BOX 09/01/2026 2 5 in 1 POUCH 2 0.624 g in 1 PATCH; Type 0: Not a Combination Product 3 NDC:71590-012-30 6 in 1 BOX 09/01/2026 3 5 in 1 POUCH 3 0.624 g in 1 PATCH; Type 0: Not a Combination Product 4 NDC:71590-012-05 5 in 1 POUCH 09/01/2026 4 0.624 g in 1 PATCH; Type 0: Not a Combination Product 5 NDC:71590-012-10 10 in 1 POUCH 09/01/2026 5 0.624 g in 1 PATCH; 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 08/06/2025 Labeler - Active Intelligence, LLC (080416593) Establishment Name Address ID/FEI Business Operations Active Intelligence, LLC 080416593 manufacture(71590-012)
