Label: NEUTRAL HANDMADE PURPLE- honey soap
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Contains inactivated NDC Code(s)
NDC Code(s): 71657-0002-1 - Packager: BNS Industry Co., Ltd.
- 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.
Drug Label Information
Updated August 17, 2017
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
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PURPOSE
Neutral soap helps remove dead skin by finding deeper skin wastes.
Removes fine dust and heavy metals from the skin.
PH 4.5 ~ 5.5 and the closest hydrogen ion concentration pH 7 ~ 7.99 neutral soap provides skin elasticity, enhances moisturizing effect and keeps skin smooth.
The soap conatains 20% natural fermentation and herbal extracts.
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
Precautions when using
1. Non-spreading neutral soap is rich in vitamins, minerals, and proteins in over 10 herbs that are beneficial to your skin and balance.
2. If there is a lot of harmful substances on the skin layer, it may be tingling at first use, but if you use it repeatedly, you may feel comfortable.
3. Professional consultation may be needed If the skin is steroid.
4. This product can be compensated according to the consumer injury compensation rule.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NEUTRAL HANDMADE PURPLE
honey soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71657-0002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HONEY (UNII: Y9H1V576FH) (HONEY - UNII:Y9H1V576FH) HONEY 9 g in 110 g Inactive Ingredients Ingredient Name Strength ORANGE OIL (UNII: AKN3KSD11B) LAVENDER OIL (UNII: ZBP1YXW0H8) LEMON OIL (UNII: I9GRO824LL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71657-0002-1 110 g in 1 BOX; Type 0: Not a Combination Product 08/17/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/17/2017 Labeler - BNS Industry Co., Ltd. (688460696) Registrant - BNS Industry Co., Ltd. (688460696) Establishment Name Address ID/FEI Business Operations BNS Industry Co., Ltd. 688460696 label(71657-0002) , manufacture(71657-0002) , pack(71657-0002)
