VALTRUM IMMEDIATE ACTION TOPICAL ANALGESIC- camphor, menthol, methyl salicylate cream

Valtrum IMMEDIATE ACTION TOPICAL ANALGESIC by

Drug Labeling and Warnings

Valtrum IMMEDIATE ACTION TOPICAL ANALGESIC by is a Otc medication manufactured, distributed, or labeled by LABORATORIOS QUANTIUM LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Camphor 3%
Menthol 3%
Methyl salicylate 10%

Purpose

Topical analgesic

Uses

For the temporary relief of minor aches and pains of muscles and joints associated with Simple Backache Arthritis Strains Bruises Sprains

Warnings

For external use only

Avoid contact with eyes and mucous membranes Do not use otherwise than as directed.
Caution: Discontinue use if excessive irritation of the skin develops.

When using this product:  Do not bandage tightly  Do not apply to wounds or damaged skin.

Stop use and ask a doctor if:  Conditions worsens  Symptoms persist for more than 7 days or clear up and occur again within a few days.

If pregnant or breast-feeding, ask a health professional before use.

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

Directions

Adults and Children 18 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 18 years of age: Consult a doctor.

Other information

Store in a cool dry place away from direct sunlight Keep lid tightly closed

Inactive Ingredients:

Cetyl Stearyl Alcohol, DMDM Hydantoin, Glucosamine Sulfate, Mineral Oil, PEG-20 Cetyl/Stearyl Ether, Polysorbate 20, Purified Water, Sodium Hydroxide, Stearyl Alcohol, Tocopheryl Acetate.

SPL UNCLASSIFIED SECTION

POWERFUL ANALGESIC

NEW CREAM

santo remedio

info@quantiumlab.com

www.valtrum-santoremedio.com

Packaging

INGREDIENTS AND APPEARANCE

VALTRUM IMMEDIATE ACTION TOPICAL ANALGESIC 
camphor, menthol, methyl salicylate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75849-897
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	3 g  in 100 g
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	3 g  in 100 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
DMDM HYDANTOIN (UNII: BYR0546TOW)
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
MINERAL OIL (UNII: T5L8T28FGP)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75849-897-03	90 g in 1 TUBE; Type 0: Not a Combination Product	01/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	01/01/2024

Labeler - LABORATORIOS QUANTIUM LLC (027101451)