Label: NELLY DEVUYST MASK BIOACNE- salicylic acid cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71447-005-01 - 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 Ingredients
- 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
▪ For new users: apply product to a small area once to test if you are sensitive to this product.
▪ If no discomfort occurs, apply a thin layer to face, let dry five minutes or until mask turns white. After mask has dried, rinse thoroughly. Pat dry with towel. Use 1-2 times per week.
▪ If dryness or peeling occurs, reduce frequency of application.
- Other information
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Inactive ingredients
Aloe Barbadensis Leaf Juice*, Kaolin, Arctium Lappa Root Extract*, Urtica Dioica (Nettle) Extract*, Lavandula Angustifolia (Lavender) Flower Extract*, Propanediol, Silica, Glycerin, Coco-Glycoside, Sea Silt, 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*, Tocopherol, Bentonite, Carrageenan, Sodium Gluconate, Levulinic Acid, Sodium Levulinate, Sodium Carboxymethyl Cellulose, Sodium Anisate, Xanthan Gum, Potassium Sorbate, Citric Acid, Aqua.
Certified organic*
- Questions or Comments?
- Distributed By
- NELLY DEVUYST MASK BIOACNE 5.20 OZ. (150g) (71447-005-01)
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INGREDIENTS AND APPEARANCE
NELLY DEVUYST MASK BIOACNE
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71447-005 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 ZINC OXIDE (UNII: SOI2LOH54Z) LAVANDIN OIL (UNII: 9RES347CKG) TEA TREE OIL (UNII: VIF565UC2G) MICHELIA ALBA LEAF OIL (UNII: 002RK9L1FN) CITRUS AURANTIIFOLIA FRUIT OIL (UNII: 7937R189CB) ALOE VERA LEAF (UNII: ZY81Z83H0X) KAOLIN (UNII: 24H4NWX5CO) CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T) BENTONITE (UNII: A3N5ZCN45C) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) XANTHAN GUM (UNII: TTV12P4NEE) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) WATER (UNII: 059QF0KO0R) SEA SALT (UNII: 87GE52P74G) SILVER CITRATE (UNII: CKA421A1J7) MAGNOLIA OFFICINALIS BARK (UNII: 5M609NV974) TOCOPHEROL (UNII: R0ZB2556P8) CARRAGEENAN (UNII: 5C69YCD2YJ) SODIUM GLUCONATE (UNII: R6Q3791S76) LEVULINIC ACID (UNII: RYX5QG61EI) SODIUM LEVULINATE (UNII: VK44E1MQU8) URTICA DIOICA LEAF (UNII: X6M0DRN46Q) LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M) PROPANEDIOL (UNII: 5965N8W85T) ARCTIUM LAPPA ROOT OIL (UNII: 55DGS3F5YG) GLYCERIN (UNII: PDC6A3C0OX) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) COCO GLUCOSIDE (UNII: ICS790225B) SODIUM ANISATE (UNII: F9WFJ28MV9) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71447-005-01 150 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 INC 203095039 pack(71447-005) Establishment Name Address ID/FEI Business Operations LABORATOIRES DRUIDE INC 245815014 manufacture(71447-005) , label(71447-005)