Label: GD11 RX SCM C5- mannitol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 62171-100-01, 62171-100-02 - Packager: Coson Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated August 24, 2017
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
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WARNINGS
Warnings: For external use only
Caution in usage 1. In case of having problems such as red rash, swollenness, itching, you need to consult a dermatologist. 2. You are banned to use it on the part where you have a scar, eczema, or dermatitis 3. Caution for treatment and keeping. - Keep it out of infants or children's reach. - Don't keep it exposed to the direct sunlight
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GD11 RX SCM C5
mannitol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62171-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MANNITOL (UNII: 3OWL53L36A) (MANNITOL - UNII:3OWL53L36A) MANNITOL 0.10 g in 2 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Betaine (UNII: 3SCV180C9W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62171-100-02 10 in 1 CARTON 07/01/2017 1 NDC:62171-100-01 2 mL in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/01/2017 Labeler - Coson Co., Ltd. (689835593) Registrant - Coson Co., Ltd. (689835593) Establishment Name Address ID/FEI Business Operations COSON Co., Ltd._Osan Plant 689847210 manufacture(62171-100)