ABSORBINE BACK THERAPEUTIC PAIN RELIEF- menthol patch

Absorbine BACK Therapeutic Pain Relief by

Drug Labeling and Warnings

Absorbine BACK Therapeutic Pain Relief by is a Otc medication manufactured, distributed, or labeled by Teh Seng Pharmaceutical Mfg. Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Absorbine BACK PATCH Therapeutic Pain Relief

Active ingredient

Menthol 5%

Purpose

Topical analgesic

Uses

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

• simple backache
• arthritis
• sprains
• strains
• bruises

Warnings

For external use only

THIS PRODUCT CONTAINS NATURAL RUBBER LATEX WHICH MAY CAUSE ALLERGIC REACTIONS

Do not use

• on wounds or damaged skin
• with a heating pad

Ask a doctor before use if you have

• redness over affected area

When using this product

• avoid contact with eyes and mucous membranes
• do not bandage tightly

Stop use and ask a doctor if

• condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days
• excessive skin irritation occurs

Keep out of reach of children.

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

Directions

• adults and children 12 years of age and older apply to the affected area no more than 3 to 4 times daily
• open pouch & remove patch
• stretch & peel off protective film and apply sticky side to affected area
• children under 12 years of age consult a doctor

Inactive ingredients

adhesive plaster, aloe barbadensis gel, aluminum chlorohydrate, dl-camphor, menthol oil, paraffin oil, purified lanolin, silicon dioxide, spearmint, titanium dioxide, zinc oxide

Absorbine BACK PATCH Therapeutic Pain Relief 18 Count (

67536-223-01)| Absorbine BACK PATCH Therapeutic Pain Relief 36 Count (67536-223-02)

INGREDIENTS AND APPEARANCE

ABSORBINE BACK THERAPEUTIC PAIN RELIEF 
menthol patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67536-223
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
MINERAL OIL (UNII: T5L8T28FGP)
LANOLIN (UNII: 7EV65EAW6H)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SPEARMINT (UNII: J7I2T6IV1N)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
ZINC OXIDE (UNII: SOI2LOH54Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67536-223-01	18 in 1 PACKAGE	10/10/2013	03/31/2021
1		8.8 g in 1 PATCH; Type 0: Not a Combination Product
2	NDC: 67536-223-02	36 in 1 PACKAGE	10/10/2013	04/30/2021
2		8.8 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 not final	part348	10/10/2013	04/30/2021

Labeler - Teh Seng Pharmaceutical Mfg. Co., Ltd. (656347721)

Establishment
Name	Address	ID/FEI	Business Operations
Teh Seng Pharmaceutical Mfg. Co., Ltd.		656347721	manufacture(67536-223)