Label: NELLY DEVUYST SERUM BIOACNE- salicylic acid liquid
- NDC Code(s): 71447-006-00
- Packager: LABORATOIRES DRUIDE INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 January 1, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DRUG FACTS
- Active Ingredients
- Purpose
- Uses
- Warnings
- When using this product
- Stop use
- and ask a doctor
- Keep out of reach of children
-
Directions
▪ Cleanse skin thoroughly before applying the product.
▪ For new users: apply product to a small area once a day for three days to test if you are sensitive to this product.
▪ If no discomfort occurs, cover the entire affected area with a thin layer.
▪ Start with one application daily, then gradually increase to two or three times daily, if needed.
▪ If dryness or peeling occurs, reduce application to once a day or every other day.
- Other information
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Inactive Ingredients
Thymus Vulgaris (Thyme) Extract*, Alcohol, Arctium Lappa Root Extract*, Urtica Dioica (Nettle) Extract*, Lavandula Angustifolia (Lavender) Flower Extract*, Propanediol, Silver Citrate, Magnolia Officinalis Bark Extract, Michelia Alba Flower Oil, Citrus Aurantifolia (Lime) Oil*, Lavandula Hybrida Oil*, Tea Tree Leaf Oil*, Citrus Aurantium Dulcis (Orange) Peel Oil Expressed*, Arginine, Levulinic Acid, Sodium Levulinate, Potassium Sorbate, Citric Acid, Aqua.
Certified organic*
- Questions or Comments?
- Distributed By
- NELLY DEVUST SERUM BIOACNE 0.5 FL.OZ (15mL) (71447-006-00)
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INGREDIENTS AND APPEARANCE
NELLY DEVUYST SERUM BIOACNE
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71447-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 g Inactive Ingredients Ingredient Name Strength LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M) TEA TREE OIL (UNII: VIF565UC2G) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SILVER CITRATE (UNII: CKA421A1J7) MAGNOLIA OFFICINALIS BARK (UNII: 5M609NV974) MICHELIA ALBA LEAF OIL (UNII: 002RK9L1FN) SODIUM LEVULINATE (UNII: VK44E1MQU8) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PROPANEDIOL (UNII: 5965N8W85T) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) URTICA DIOICA LEAF (UNII: X6M0DRN46Q) WATER (UNII: 059QF0KO0R) THYMUS VULGARIS LEAF (UNII: GRX3499643) LAVANDIN OIL (UNII: 9RES347CKG) ALCOHOL (UNII: 3K9958V90M) LIME OIL (UNII: UZH29XGA8G) CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T) ARGININE (UNII: 94ZLA3W45F) LEVULINIC ACID (UNII: RYX5QG61EI) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71447-006-00 2 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/23/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 04/20/2018 Labeler - LABORATOIRES DRUIDE INC (245815014) Registrant - LABORATOIRES DRUIDE INC (245815014) Establishment Name Address ID/FEI Business Operations Laboratoires Druide Inc 245815014 manufacture(71447-006) , label(71447-006)