UP AND UP ULTRA STRENGTH PAIN RELIEVING (camphor- synthetic, menthol, methyl salicylate cream

Up and Up Ultra Strength Pain Relieving by

Drug Labeling and Warnings

Up and Up Ultra Strength Pain Relieving by is a Otc medication manufactured, distributed, or labeled by Target Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Camphor, 4%

Menthol, 10%

Methyl Salicylate, 30%

Purpose

Topical Analgesic

Uses

the temporary relief of minor aches and pains of muscles and joints associated with:  simple backache  arthritis  strains  bruises  sprains helps to temporarily relieve minor aches, joint discomfort and muscle pain.

Warnings

For external use only.

Do not use

• other than as directed
• with a heating pad (may blister skin)
• on children under 12 years of age

When using this product

• avoid contact with eyes or mucous membranes
• do not apply to wounds or damaged skin
• do not bandage tightly

Stop use and ask a doctor if

condition worsens

• symptoms persist for more than 7 days or clear up and occur again within a few days
• skin redness or excessive irritation of the skin develops.

Keep out of reach of children.

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

Directions

• Adults and children over 12 years
• apply to affected area no more than 3-4 times daily
• Children 12 years or younger: ask a doctor.

Other information

• store at 20-25 C (68-77 F)
• Lot # & Exp. date: see crimp of tube or see box

Inactive ingredients

carbomer, edetate disodium, glyceryl stearate, lanolin, PEG-100 stearate, polysorbate 80, potassium hydroxide, purified water, stearic acid, trolamine.

Package Labeling:

INGREDIENTS AND APPEARANCE

UP AND UP ULTRA STRENGTH PAIN RELIEVING 
camphor (synthetic), menthol, methyl salicylate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-960
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	100 mg  in 1 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	100 mg  in 1 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	300 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
LANOLIN (UNII: 7EV65EAW6H)
PEG-100 STEARATE (UNII: YD01N1999R)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
WATER (UNII: 059QF0KO0R)
STEARIC ACID (UNII: 4ELV7Z65AP)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-960-01	1 in 1 BOX	03/01/2018
1		113 g in 1 TUBE; 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	03/01/2018

Labeler - Target Corporation (006961700)