Label: DIAL COMPLETE ADVANCED MOISTURE SPRING WATER- dial complete advanced moisture spring water fhw solution
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Contains inactivated NDC Code(s)
NDC Code(s): 50663-342-01, 50663-342-02 - Packager: Zotos International Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 November 9, 2020
If you are a consumer or patient please visit this version.
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- Drug Facts
- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask doctor if
- Keep out of reach of children.
- Directions
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Inactive ingredients
Advanced Moisture Spring Water FHW
Aqua (Water, Eau) · Lauramidopropylamine Oxide · Cetrimonium Chloride · Glycerin · Lauramine Oxide · Citric Acid · Cocamidopropyl Betaine · Trideceth-9 · Sodium Benzoate · Myristamidopropylamine Oxide · PEG-5 Isononanoate · Parfum (Fragrance) · Zinc Sulfate · Sodium Chloride · Dimethyl Lauramine · Tetrasodium EDTA · Alcohol · Dimethyl Myristamine · CI 42090 (Blue 1) · CI 17200 (Red 33)
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- INDICATIONS & USAGE
- Topical Liquid Solution
- 4 Pack
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INGREDIENTS AND APPEARANCE
DIAL COMPLETE ADVANCED MOISTURE SPRING WATER
dial complete advanced moisture spring water fhw solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50663-342 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 91.51 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50663-342-01 1180 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/01/2020 2 NDC:50663-342-02 3780 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 11/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 11/01/2020 Labeler - Zotos International Inc (966706145)