ABSORBINE JR.- menthol liquid 
W. F. Young, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Absorbine
jr.®
PAIN RELIEF LIQUID

Drug Facts

Active ingredient

Natural menthol 1.27%

Purpose

Topical analgesic

Uses

for temporary relief of minor aches and pains of muscles and joints associated with:

  • arthritis
  • simple backache
  • sprains
  • strains
  • bruises

Warnings

For external use only

Flammable

  • keep away from fire, sparks and heated surfaces

Do not use

  • on wounds or damaged skin

When using this product

  • do not bandage tightly
  • avoid contact with eyes

Stop use and ask a doctor if

  • condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • adults and children 2 years of age and older: apply to the affected area no more than 3 to 4 times daily
  • children under 2 years of age; consult a doctor

Inactive ingredients

absinthium oil, acetone, chloroxylenol, FD&C blue no. 1, FD&C yellow no. 6, iodine, plant extracts of calendula, echinacea, and wormwood; potassium iodide, thymol, and water

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Carton

Absorbine jr.®
PAIN RELIEF LIQUID

FAST
and
STRONG

RAPID
RELIEF
for Sore Muscles
& Arthritis Pain

Fast Absorbing

Deep Penetrating
Relief

Non-Greasy

NO-MESS APPLICATOR

LIQUID

4 FL. OZ. (118 mL)

Principal Display Panel - 118 mL Carton
ABSORBINE JR. 
menthol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11444-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Menthol (UNII: L7T10EIP3A) (Menthol - UNII:L7T10EIP3A) Menthol0.0127 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Acetone (UNII: 1364PS73AF)  
Chloroxylenol (UNII: 0F32U78V2Q)  
FD&C Blue no. 1 (UNII: H3R47K3TBD)  
FD&C Yellow no. 6 (UNII: H77VEI93A8)  
Iodine (UNII: 9679TC07X4)  
Calendula Officinalis Flower (UNII: P0M7O4Y7YD)  
echinacea, unspecified (UNII: 4N9P6CC1DX)  
wormwood (UNII: F84709P2XV)  
potassium iodide (UNII: 1C4QK22F9J)  
thymol (UNII: 3J50XA376E)  
water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11444-001-031 in 1 CARTON
159.2 mL in 1 BOTTLE, PLASTIC
2NDC:11444-001-041 in 1 CARTON
2118 mL in 1 BOTTLE, PLASTIC
3NDC:11444-001-06473 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34801/01/190102/28/2018
Labeler - W. F. Young, Inc. (001114669)

Revised: 9/2013
 
W. F. Young, Inc.