TLC Plus Anesthetic Gel

Manufacturer
Renu Laboratories, Inc.
Effective date
2022-01-18
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 22:13:47

Label at a glance#

ProductTLC Plus Anesthetic G
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure12 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Directions: adults and children over 12 years

  • apply a thin layer to affected area every 6 to 8 hours
  • after applying, wash hands with soap and water

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Lidocaine HCl 4%

OTC - STOP USE SECTION

Stop Use and ask a doctor if:

  • condition worsens
  • redness is present
  • irritation develops
  • symptoms persist for more then 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 product was applied.

OTC - ASK DOCTOR SECTION

Stop Use and ask a doctor if:

condition worsens
redness is present
irritation develops
symptoms persist for more then 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 product was applied.

OTC - DO NOT USE SECTION

Do not use

  • on large areas of the body or on cut, irritated or swollen skin
  • on puncture wounds
  • for more than one week without consulting a doctor

INDICATIONS & USAGE SECTION

Uses

For the temporary relief of pain associated with minor skin procedures

OTC - PURPOSE SECTION

Topical Anesthetic

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding,

ask a health professional

before use

WARNINGS SECTION

Warnings

For external use only

Do not use

  • on large areas of the body or on red, irritated or swollen skin
  • on puncture wounds
  • for more than one week wihout consulting a doctor

INACTIVE INGREDIENT SECTION

Aloe Leaf Powder, Benzyl Alcohol, Deionized Water, Disodium EDTA, Ethyl Alcohol, Glycerin,

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep ot of reach of children

and pets.

If swallowed, get medical help or contact a Poison Control Center right away.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

JAR BOTTOM_LABELJAR BOTTOM_LABELJAR SIDEJAR SIDE

Products#

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DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76348-41676348-416-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
e6d58e9b-161f-15c1-e053-2995a90a43a54d0fc18f-1381-5103-e054-00144ff88e882022-08-22WarningsExact identifier
spl set id: 4d0fc18f-1381-5103-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.