Label: DR.NUELL MUGWORT SHAKING PACK- glycerin liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 73430-0002-1 - Packager: Apharm Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 2, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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INDICATIONS & USAGE
1. put 1st and 2nd packs in the pouch and seal them and shake them for 10 seconds
2. sweep the contents down and tear them along the bottom cut line
3. apply mixture to the fact with a sqag-hola and gently remove it from the bottom to the top after 20~30 minutes
4. remove the pack and apply skin product
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WARNINGS
1) if there is any abnormal symptom or side effect, such as red spot, swelling and itching when using cosmetlcs or after using due to direct sunlight, consult dermatologists
2) Do not use for wounded areas
3) Precautions for storage and handling
keep out of reach of children, store away from direct sunlight
4) avoid the eye area - INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR.NUELL MUGWORT SHAKING PACK
glycerin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73430-0002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 5.021 g in 100 g Inactive Ingredients Ingredient Name Strength ALLANTOIN (UNII: 344S277G0Z) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73430-0002-1 70 g in 1 PACKAGE; Type 0: Not a Combination Product 11/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part347 11/01/2019 Labeler - Apharm Co., Ltd. (689054266) Registrant - Apharm Co., Ltd. (689054266) Establishment Name Address ID/FEI Business Operations APHARM Co., Ltd. 689054266 manufacture(73430-0002)
