VEIURKIU EXTERNAL ANALGESIC CREAM- lidocaine cream

Veiurkiu External Analgesic Cream by

Drug Labeling and Warnings

Veiurkiu External Analgesic Cream by is a Otc medication manufactured, distributed, or labeled by BLOOMWELL GARDENS LLC, Jiangxi Hemei Pharmaceutical Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Lidocaine 4%

INACTIVE INGREDIENT

Water, Propylene Glycol, Carbomer Homopolymer, Glycerin,

Edetate Disodium, Hydroxyacetophenone, 1,2-Hexanediol,

Mentha Arvensis Leaf, Chrysanthemum Indicum Top,

Portulaca, Polyoxyl 40 Hydrogenated Castor Oil

PURPOSE

Temporary relief of minor aches and pains

INDICATIONS & USAGE

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

Flammable: keep away from fire or flame

STOP USE

Stop use and ask a doctor if: condition worsens

symptoms persist for more than 7 days

symptoms clear up and occur again within a few days

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or

contact a Poison Control Center right away.

PREGNANCY OR BREAST FEEDING

If pregnant or breastfeeding, ask a health professional before use

DO NOT USE

Do not use: on wounds or damaged skin with a heating pad

if allergic to menthol or any ingredient in this product

WHEN USING

When using this product: avoid contact with eyes,

mucous membranes do not bandage tightly

DOSAGE & ADMINISTRATION

Directions

Adults and children 12 years and older: apply to affected area

not more than 3 to 4 times daily

Children under 12 years: ask a doctor

OTHER SAFETY INFORMATION

Store at 15–30°C (59–86°F)

Protect from excessive moisture and direct sunlight

Keep the carton for full labeling

PRINCIPAL DISPLAY PANEL

Package Label Principal Display Panel

INGREDIENTS AND APPEARANCE

VEIURKIU EXTERNAL ANALGESIC CREAM 
lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85284-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
PORTULACA GRANDIFLORA WHOLE (UNII: 58DNV0B13N)
EDETATE DISODIUM (UNII: 7FLD91C86K)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
CHRYSANTHEMUM INDICUM TOP (UNII: 607YAE70V1)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
MENTHA ARVENSIS LEAF (UNII: A4IWO4DDZ9)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85284-011-01	50 g in 1 BOTTLE; Type 0: Not a Combination Product	10/12/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	10/12/2025

Labeler - BLOOMWELL GARDENS LLC (124839891)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd.		724892056	manufacture(85284-011)