Label: ABSORBINE JR PRO NO MESS ROLL-ON PLUS- lidocaine hcl, phenol cream
- NDC Code(s): 69693-419-25
- Packager: Clarion Brands, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 21, 2023
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- Active Ingredients
- Purpose
- Use
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- If pregnant or breast feeding,
- Keep out of reach of children.
- Directions
- Inactive Ingredients
- Questions?
-
Principal Display Panel
ABSORBINE® jr.
QUALITY RELIEF SINCE 1903
PRO
PAIN RELIEF
LIDOCAINE + PHENOL
TWO MAX STRENGTH PAIN RELIEVERStDEEP PENETRATING
PAIN RELIEF
2X MORE
POWERED BY 2 MAX STRENGTH INGREDIENTS*
FAST ACTING - LONG LASTING
ROLL ON
NET WT 2.5 OZ (70 g)
ABSORBINE PRO™ jr.
Max Numbing Pain Relief†
Uniquely formulated
with 4% LIDOCAINE &
1.5% PHENOL, making
PRO the only pain
reliever with two
maximum strength
anesthetics.†
The DUAL ACTION
FORMULA delivers
fast acting, deep
penetrating pain relief.
LIDOCAINE
BLOCKS
PAIN SIGNALS
TO THE BRAIN
PHENOL
NUMBS
NERVES
Keep carton as it contains important information.
Distributed by:
Absorbine Jr. LLC, 811 Broad Street, Suite 600
Chattanooga, TN 37402
©2004
DEEP PENETRATING
to numb pain away
DUAL ACTION FORMULA
with max strength
Lidocaine & Phenol
for maximum numbing
relief†
COOLING POWER
for fast acting relief
*vs. single lidocaine ingredient formula alone
†in the pain relief category without a prescription
1000195
ABSORBINE® jr.
QUALITY RELIEF SINCE 1903
PRO
PAIN RELIEF
LIDOCAINE + PHENOL
TWO MAX STRENGTH PAIN RELIEVERS†
2X MORE
POWERED BY 2 MAX STRENGTH INGREDIENTS*
FAST ACTING - LONG LASTING
ROLL ON NET WT 2.5 OZ (70 g)For more information, visit
www.Absorbine Jr.com
Distributed by: Absorbine Jr. LLC
811 Broad Street, Suite 600, Chattanooga, TN 37402
©2004
*vs. Single Lidocaine Ingredient Formula Alone
†without a prescription
Child resistant packaging. Replace cap after each use.
1000204
-
INGREDIENTS AND APPEARANCE
ABSORBINE JR PRO NO MESS ROLL-ON PLUS
lidocaine hcl, phenol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69693-419 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 Phenol (UNII: 339NCG44TV) (Phenol - UNII:339NCG44TV) Phenol 15 mg in 1 g Inactive Ingredients Ingredient Name Strength Aloe Vera Leaf (UNII: ZY81Z83H0X) Aminomethylpropanol (UNII: LU49E6626Q) Levomenol (UNII: 24WE03BX2T) Camphor Leaf Oil (UNII: 51D0RGY52V) Glycerin (UNII: PDC6A3C0OX) Hydroxyethyl Cellulose, Unspecified (UNII: T4V6TWG28D) Alcohol (UNII: 3K9958V90M) Mentha Arvensis Leaf Oil (UNII: 1AEY1M553N) Water (UNII: 059QF0KO0R) Ginger (UNII: C5529G5JPQ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69693-419-25 1 in 1 CARTON 02/15/2023 1 70 g in 1 BOTTLE, WITH APPLICATOR; 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 02/15/2023 Labeler - Clarion Brands, LLC (079742703)