Label: RUIGOO MINOXIDIL TOPICAL GEL- minoxidil 5% gel
- NDC Code(s): 83767-101-01, 83767-101-02
- Packager: Guangzhou Ruijiu Electronic Technology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 9, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
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DO NOT USE
Your degree of hair loss is different than that shown on side of this cartonbecause this product may not work for you.
Your hair loss is sudden and/or patchy
You are under 18 years of age. Do not use on babies or children
Your scalp is red, inflamed, infected, irritated, or painful
You use other medicines on the scalp -
WHEN USING
Do not use more than directed.
Avoid contact with the eyes, ears, and mouth. In case of accidental contact, rinse eyes with large amounts of cool tap water.
lt takes time to regrow hair. Results may occur at 2 months with once dailyuse. For some individuals, it may take at least 4 months before resultsbecome noticeable.
The amount of hair regrowth is different for each person. This product will not work for all women. - STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
RUIGOO MINOXIDIL TOPICAL GEL
minoxidil 5% gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83767-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 5 g in 100 mL Inactive Ingredients Ingredient Name Strength CETYL ALCOHOL (UNII: 936JST6JCN) GLYCERIN (UNII: PDC6A3C0OX) POLYSORBATE 80 (UNII: 6OZP39ZG8H) STEARIC ACID (UNII: 4ELV7Z65AP) SORBITAN MONOOLEATE (UNII: 06XEA2VD56) OLEIC ACID (UNII: 2UMI9U37CP) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83767-101-02 1 in 1 CARTON 10/26/2023 1 NDC:83767-101-01 100 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 10/26/2023 Labeler - Guangzhou Ruijiu Electronic Technology Co., Ltd. (631973699) Registrant - Guangzhou Ruijiu Electronic Technology Co., Ltd. (631973699) Establishment Name Address ID/FEI Business Operations Guangzhou Ruijiu Electronic Technology Co., Ltd. 631973699 manufacture(83767-101)