PUVIDA NUMBING (menthol 5%- w/w numbing cream

PUVIDA NUMBING by

Drug Labeling and Warnings

PUVIDA NUMBING by is a Otc medication manufactured, distributed, or labeled by Jiangxi Yudexi Pharmaceutical Co., LTD, Jiangxi Zhongletang Pharmaceuticals Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Menthol 5% (w/w)

Purpose

External analgesic

Use

For the temporary relief of pain and itching associated with minor burns, sunburn, insect bites and minor skin irritation

Warnings

·For external use only
·If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor
·Do not use in large quantities, particularly over raw surfaces or blistered areas
·Avoid contact with eyes. If this happens, rinse thoroughly with water

Do not use

·Do not use in large quantities, particularly over raw surfaces or blistered areas

When Using

·Avoid contact with eyes, lf this happens, rinse thoroughly with water.

Stop Use

·Condition worsens or does not improve within 7 days
·Allergic reaction occurs to ingredients in this product
·Symptom being treated does not subside or if redness, irritation

Ask Doctor

·Condition worsens or does not improve within 7 days
·Allergic reaction occurs to ingredients in this product
·Symptom being treated does not subside or if redness, irritation

Keep Oot Of Reach Of Children

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

Directions

Adults and children 2 years of age and older:
Apply to affected area not more than 3 to 4 times daily.
Children under 2 years of age: Do not use, consult a doctor

Other information

Store between 15-30℃(59-86F). Avoid freezing and excessive heat above 40 ℃(104°F).

Inactive ingredients

Water, Carbomer 934, Propylene Glycol, Soybean Lecithin, Alpha-Tocopherol Acetate, Benzyl Alcohol.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PUVIDA NUMBING 
menthol 5% (w/w) numbing cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85248-172
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
BENZYL ALCOHOL (UNII: LKG8494WBH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SOYBEAN LECITHIN (UNII: 1DI56QDM62)
CARBOMER 934 (UNII: Z135WT9208)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85248-172-01	50 g in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	03/26/2026

Labeler - Jiangxi Yudexi Pharmaceutical Co., LTD (455662836)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Zhongletang Pharmaceuticals Co.,Ltd		411295811	manufacture(85248-172)