SWIFTALYN NUMBING CREAM- menthol 1% cream

Swiftalyn Numbing Cream by

Drug Labeling and Warnings

Swiftalyn Numbing Cream by is a Otc medication manufactured, distributed, or labeled by GENUINE INNOVATION LTD, Jiangxi Zhongletang Pharmaceuticals Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Menthol 1%

PURPOSE

Topical Analgesic

INDICATIONS & USAGE

Temporary relief of minor aches and pains of muscles and joints

WARNINGS

For external use only ■ avoid contact with eyes or mucous membranes ■ Use only as directed ■ condition worsens or does not improve within 7 days ■ allergic reaction occurs to ingredients in this product ■ symptoms being treated do not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase
If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

DOSAGE & ADMINISTRATION

■ Adults: When practical, clean and dry the affected area. Apply externally to the affected area up to 3 times daily. ■ Children under 12 years of age: consult a doctor.

OTHER SAFETY INFORMATION

■ Store at room temperature 15–30°C (59–86°F) ■ Keep away from direct sunlight or heat

INACTIVE INGREDIENT

Water, Propylene Glycol, Glycerin, Caprylic/Capric Triglyceride, Lecithin, Polysorbate 80, Aloe Vera Leaf Juice, Carbomer, Triethanolamine, Tocopheryl Acetate, Allantoin, Menthol, Phenoxyethanol, Ethylhexylglycerin.

QUESTIONS

Email at: service@swiftalyn.co.uk

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SWIFTALYN NUMBING CREAM 
menthol 1% cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87013-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL	1 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
TOCOPHEROL (UNII: R0ZB2556P8)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
ALLANTOIN (UNII: 344S277G0Z)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
CARBOMER (UNII: 0A5MM307FC)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87013-003-01	50 g in 1 CARTON; Type 0: Not a Combination Product	02/23/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	02/23/2026

Labeler - GENUINE INNOVATION LTD (226088244)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Zhongletang Pharmaceuticals Co., Ltd.		411295811	manufacture(87013-003)