Label: FACE-BODY-S- potassium carbonate liquid
- NDC Code(s): 71957-0003-1
- Packager: NARO, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Updated January 1, 2018
If you are a consumer or patient please visit this version.
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
Keep out of reach of childrenClose
- INDICATIONS & USAGE
Spray on skin as neededClose
For external use only
Do not use when liquid comes in contact with eyes, rinse immediately with water and consult the doctor.
When using this product
- Do not apply on other parts of the body
- Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Store at room temperatureClose
- DOSAGE & ADMINISTRATION
For external use onlyClose
- INGREDIENTS AND APPEARANCE
potassium carbonate liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71957-0003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE 0.1 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71957-0003-1 80 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/02/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/02/2018 Labeler - NARO, INC. (694590211) Registrant - NARO, INC. (694590211) Establishment Name Address ID/FEI Business Operations NARO, INC. 694590211 manufacture(71957-0003)