Label: DOITU ACNE MICROCRYSTALLINE INVISIBLE ACNE PATCH (salix alba (willow) bark extract, menthol, aesculus chinensis extract, bisabolol, zingiber officinale- ginger root extract patch
-
Contains inactivated NDC Code(s)
NDC Code(s): 83093-101-03 - Packager: Guangdong ZhiZhen Biological Medicine Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated November 24, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
-
WHEN USING
■Apply to affected areas only
■Avoid unnecessary sun exposure
■Do not use in or near the eyes
■When most of the acne patches are white, they can be replaced
■When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. - STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
Directions
Before use, it is recommended to clean the acne area on the face first. After the skin is dry, tear off an acne patch from the film, align it with the center of the acne, gently stick it on the acne, and gently press it with the finger pulp to make it stick. If you need to make up, please use the acne patch first and then apply makeup.
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DOITU ACNE MICROCRYSTALLINE INVISIBLE ACNE PATCH
salix alba (willow) bark extract, menthol, aesculus chinensis extract, bisabolol, zingiber officinale (ginger) root extract patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83093-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.72 mg in 40 mg LEVOMENOL (UNII: 24WE03BX2T) (LEVOMENOL - UNII:24WE03BX2T) LEVOMENOL 0.02388 mg in 40 mg GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ) GINGER 0.00012 mg in 40 mg AESCULUS CHINENSIS WHOLE (UNII: PGU072XJ6U) (AESCULUS CHINENSIS WHOLE - UNII:PGU072XJ6U) AESCULUS CHINENSIS WHOLE 0.00312 mg in 40 mg SALIX ALBA BARK (UNII: 205MXS71H7) (SALIX ALBA BARK - UNII:205MXS71H7) SALIX ALBA BARK 0.8 mg in 40 mg Inactive Ingredients Ingredient Name Strength STYRENE/ISOPRENE/STYRENE BLOCK COPOLYMER (UNII: K7S96QM8DV) 5.67 mg in 40 mg CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) 17.01 mg in 40 mg POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52) 15.12 mg in 40 mg CYCLODEXTRINS (UNII: 7E6SK9QDT8) 0.04488 mg in 40 mg PICHIA JADINII (UNII: 8JRL032K80) 0.6 mg in 40 mg HYALURONATE SODIUM (UNII: YSE9PPT4TH) 0.008 mg in 40 mg Product Characteristics Color Score Shape ROUND Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83093-101-03 40 mg in 1 PATCH; Type 0: Not a Combination Product 11/25/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/25/2022 Labeler - Guangdong ZhiZhen Biological Medicine Co., Ltd. (712547927) Registrant - Guangdong ZhiZhen Biological Medicine Co., Ltd. (712547927) Establishment Name Address ID/FEI Business Operations Guangdong ZhiZhen Biological Medicine Co., Ltd. 712547927 manufacture(83093-101)
