Label: NELLY DEVUYST PURIFYING BIOACNE- salicylic acid gel
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Contains inactivated NDC Code(s)
NDC Code(s): 71447-004-01 - 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 May 26, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DRUG FACTS
- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use
- and ask a doctor if
- Keep out of reach of children
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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
Aloe Barbadensis Leaf Juice*, Propanediol, Arctium Lappa Root Extract*, Urtica Dioica (Nettle) Extract*, Lavandula Angustifolia (Lavender) Flower Extract*, Glycerin, Zinc Oxide, 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*, Bentonite, Carrageenan, Sodium Gluconate, Levulinic Acid, Sodium Levulinate, Sodium Carboxymethyl Cellulose, Sodium Anisate, Sclerotium Gum, Xanthan Gum, Tocopherol, Citric Acid, Potassium Sorbate, Aqua.
* Certified organic.
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- Distributed By
- NELLY DEVUYST PURIFYING GEL BIOACNE 5.20.OZ. (150g)
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INGREDIENTS AND APPEARANCE
NELLY DEVUYST PURIFYING BIOACNE
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71447-004 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 MICHELIA ALBA LEAF OIL (UNII: 002RK9L1FN) SILVER CITRATE (UNII: CKA421A1J7) MAGNOLIA OFFICINALIS BARK (UNII: 5M609NV974) LAVANDIN OIL (UNII: 9RES347CKG) CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T) BENTONITE (UNII: A3N5ZCN45C) CARRAGEENAN (UNII: 5C69YCD2YJ) GLYCERIN (UNII: PDC6A3C0OX) SODIUM GLUCONATE (UNII: R6Q3791S76) LEVULINIC ACID (UNII: RYX5QG61EI) SODIUM LEVULINATE (UNII: VK44E1MQU8) PROPANEDIOL (UNII: 5965N8W85T) URTICA DIOICA LEAF (UNII: X6M0DRN46Q) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) SODIUM ANISATE (UNII: F9WFJ28MV9) BETASIZOFIRAN (UNII: 2X51AD1X3T) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) TOCOPHEROL (UNII: R0ZB2556P8) LIME OIL (UNII: UZH29XGA8G) TEA TREE OIL (UNII: VIF565UC2G) LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M) ZINC OXIDE (UNII: SOI2LOH54Z) ALOE VERA LEAF (UNII: ZY81Z83H0X) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71447-004-01 150 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product 05/26/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 05/26/2018 Labeler - LABORATOIRES DRUIDE INC (245815014) Registrant - LABORATOIRES DRUIDE INC (245815014) Establishment Name Address ID/FEI Business Operations 7774672 CANADA IINC 203095039 pack(71447-004) Establishment Name Address ID/FEI Business Operations LABORATOIRES DRUIDE INC 245815014 manufacture(71447-004) , label(71447-004)
