Feel better now cream

Drug facts

Active ingredient

Lidocaine 5%


Local Anesthetic


for the temporary relief of local and anorectal discomfort associated with anorectal discomfort or inflammation.


For External use only

Do not use this product if:

  • Pregnant or breast-feeding, ask a health professional before use.
  • In case of accidental overdose, contact a doctor or Poison Control Center immediately
  • Tamper Evident "Warranty Void.. Seal.. label atop the container is broken.

When using this product:

  • Do not exceed the recommended 6 times a day.
  • In rare cases allergic reactions to ingredients in this product may occur.
  • Do not put this product into the rectum by using fingers or any mechanical device or applicator.
  • Keep out of eyes.

Stop use and ask a doctor if:

the symptom being treated does not subside or if redness, irritation, swrlling, pain or other symptoms develop or increases.

Keep out of reach of children.

In case of accidental ingestion, seek medical attention immediately.

Other information

  • Keep away from direct sunlight or heat
  • Store in room temperature (59-86 oF / 15-30 oC)


  • Adults: When practical, Cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry before application of this product.
  • Apply to small area for 15 to 25 minutes
  • Children under 12 years of age: consult a doctor

Inactive ingredients:

Water, Aloe Barbadensis Leaf Juice, Chamomilla Recutita (Matricaria) Flower Extract, Triethanolamine, Carbomer, Ethoxydiglycol, Lecithin, Neopentyl Glycol Dicaprylate/Dicaprate, Sodium Polyacrylate, Hydrogenated Polycene, Trideceth-10, Cholesterol Allantoin, Tocopheryl Acetate, Bisabolo

Ingredients and appearance - Product information

Feel better now cream- Lidocaine

Product information

Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC: 63742-005
Route of Administration Topical

Active Ingredient/Active Moiety

Ingredient Name Strength
Lidocaine ( UNII: 98PI200987)( Lidocaine - UNII: 98PI200987 ) 50 mgin 1 g

Inactive Ingredients

Ingredient Name Code
Water ( UNII: 059QF0KO0R)
Aloe vera leaf ( UNII: ZY81Z83H0X)
Chamomile ( UNII: FGL3685T2X)
Trolamine ( UNII: 9O3K93S3TK)
Carboxypolymethylene ( UNII: 0A5MM307FC)
Diethylene glycol monoethyl ether ( UNII: A1A1I8X02B)
Neopentyl glycol dicaprylate/dicaprate ( UNII: VLW429K27K)
Trideceth-10 ( UNII: G624N6MSBA)
.alpha.-tocopherol acetate ( UNII: 9E8X80D2L0)

Product Characteristics


# Item Code Package Description Marketing Start Date
1 NDC: 63742-005-00 15g in 1 BOTTLE 2018/03/01

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
OTC monograph final part346 USA 2018/03/01

Labeler - Clinical Resolution Laboratory, Inc.( 825047942)

Package labeling