MELAO ROLL-ON DEODORANT- zinc phenolsulfonate liquid

MELAO Roll-on Deodorant by

Drug Labeling and Warnings

MELAO Roll-on Deodorant by is a Otc medication manufactured, distributed, or labeled by Guangzhou Yilong Cosmetics Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Zinc Phenolsulfonate 2%

Purpose

Deodorant

Uses

Apply to underarm only and replace cap tightly after use.

WARNINGS

For external use only.

Stop use and ask a doctor if

rash occurs

Do not use

on damaged or broken skin.

When using this product

keep out of eyes. Rinse with water to remove.

Keep out of reach of children.

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

INACTIVE INGREDIENT

PARAFFIN
CETYL ALCOHOL
PEG-6 SORBITAN STEARATE
POLYSORBATE 60
WATER O-15

GLYCERIN
ETHYLHEXYL PALMITATE
XANTHAN GUM

DOSAGE & ADMINISTRATION

Apply to underarm only and replace cap tightly after use.
Do not apply to broken skin.Discontinue use if rash or irritation develops. Keep out
of reach of children.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MELAO ROLL-ON DEODORANT 
zinc phenolsulfonate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83566-295
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC PHENOLSULFONATE (UNII: 4O71YT5YB5) (ZINC CATION - UNII:13S1S8SF37)	ZINC PHENOLSULFONATE	2 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PARAFFIN (UNII: I9O0E3H2ZE)
CETYL ALCOHOL (UNII: 936JST6JCN)
PEG-6 SORBITAN STEARATE (UNII: 3453J8557N)
POLYSORBATE 60 (UNII: CAL22UVI4M)
WATER O-15 (UNII: 63M8RYN44N)
GLYCERIN (UNII: PDC6A3C0OX)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83566-295-01	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/20/2023
2	NDC: 83566-295-02	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/20/2023
3	NDC: 83566-295-03	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/20/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	12/20/2023

Labeler - Guangzhou Yilong Cosmetics Co.,Ltd. (712647107)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Yilong Cosmetics Co.,Ltd.		712647107	manufacture(83566-295)