Label: CLAIRFORE- l-ascorbic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 75768-0002-1 - Packager: ORGANELLE Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated October 31, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
For external use only.
Flammable, keep away from fire or flame.
When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.
Stop use and ask a doctor if significant irritation or sensitization develops.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLAIRFORE
l-ascorbic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75768-0002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID 5 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:75768-0002-1 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/01/2020 Labeler - ORGANELLE Inc (695719718) Registrant - ORGANELLE Inc (695719718) Establishment Name Address ID/FEI Business Operations ORGANELLE Inc 695719718 manufacture(75768-0002) , label(75768-0002)