Biotin by Shenzhen yuehaotong Technology Co.,Ltd BIOTIN liquid

Biotin by

Drug Labeling and Warnings

Biotin by is a Otc medication manufactured, distributed, or labeled by Shenzhen yuehaotong Technology Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

COMPONENTS

Salicylic acid 2%

PURPOSE

wart remover

INDICATIONS & USAGE

Apply twice daly(moring and night as a man and once as a woman.Afer apicaion, proeed with an acive masage for 3-5 minutes unthe product is fuy absorbed

WARNINGS

Forevemaluseony Avoid coniac wth eves li coniac ocus nse ihorouthly wt waier Keep out ofreach oi chidrenifvou ale preanant.nursing. otiaveanyunderving medca condion.consutyou healthcare provider before using the product

DOSAGE & ADMINISTRATION

For external use only.

DO NOT USE

Discontinue use if any irritation or adverse reaction occurs

WHEN USING

When using this product, avoid contact with eyes. lf contact occurs, rinse thoroughly with waterDiscontinue use if any irritation or adverse reaction occurs.

STOP USE

on broken or irritated scalp

KEEP OUT OF REACH OF CHILDREN

If sxralowed, get medical help or contact a Poison Conirol Cenler ngiht away.

INACTIVE INGREDIENT

Acrylates copolymer, Ethyl acetate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BIOTIN 
biotin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87492-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1)	MINOXIDIL	5 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SESAME OIL (UNII: QX10HYY4QV)
CHLORPHENESIN (UNII: I670DAL4SZ)
PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
PANTOTHENIC ACID (UNII: 19F5HK2737)
PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87492-002-01	5 mL in 1 BOX; Type 0: Not a Combination Product	03/07/2026	03/07/2031
2	NDC: 87492-002-02	15 mL in 1 BOX; Type 0: Not a Combination Product	03/07/2026	03/07/2031
3	NDC: 87492-002-03	30 mL in 1 BOX; Type 0: Not a Combination Product	03/07/2026	03/07/2031
4	NDC: 87492-002-04	50 mL in 1 BOX; Type 0: Not a Combination Product	03/07/2026	03/07/2031
5	NDC: 87492-002-05	100 mL in 1 BOX; Type 0: Not a Combination Product	03/07/2026	03/07/2031

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	03/07/2026	03/07/2031

Labeler - Shenzhen yuehaotong Technology Co.,Ltd (602067669)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen yuehaotong Technology Co.,Ltd		602067669	manufacture(87492-002)