Label: HABEN HERB F CAP- acetaminophen, dried cinnamon extract capsule
- NDC Code(s): 72988-0040-1
- Packager: Lydia Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated September 8, 2024
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- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
Warnings
For external use only.
Do not use in the eyes by putting this product into the rectum by using fingers or any mechanical device or applicator.
Ask a doctor before use if you have a vaginal discharge, rectal bleeding, diaper rash.
When using this product consult a doctor before exceeding recommended dosage.
Stop use and ask a doctor if condition gets worse, condition persists for more than 7 days, condition clears up and occurs again with within a few days. Do not begin to use any other hydrocortisone product unless you have consulted a doctor.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HABEN HERB F CAP
acetaminophen, dried cinnamon extract capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72988-0040 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CINNAMON (UNII: 5S29HWU6QB) (CINNAMON - UNII:5S29HWU6QB) CINNAMON 10 mg ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 200 mg Inactive Ingredients Ingredient Name Strength GUAIFENESIN (UNII: 495W7451VQ) SODIUM HYDROXIDE (UNII: 55X04QC32I) Product Characteristics Color white Score no score Shape CAPSULE Size 19mm Flavor Imprint Code HabenHerbF Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72988-0040-1 10 in 1 PACKAGE; Type 0: Not a Combination Product 09/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/01/2024 Labeler - Lydia Co., Ltd. (695735569) Registrant - Lydia Co., Ltd. (695735569) Establishment Name Address ID/FEI Business Operations Lydia Co., Ltd. 695735569 manufacture(72988-0040)