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    NDC 70697-0804-01 AQUARELLE 0.12 g/100mL Details

    AQUARELLE 0.12 g/100mL

    AQUARELLE is a TOPICAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by INDELPA, S.A DE C.V. The primary component is BENZALKONIUM CHLORIDE.

    Product Information

    NDC 70697-0804
    Product ID 70697-804_d57bdad7-4a59-f656-e053-2a95a90af7b2
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name AQUARELLE
    Proprietary Name Suffix n/a
    Non-Proprietary Name BENZALKONIUM CHLORIDE
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route TOPICAL
    Active Ingredient Strength 0.12
    Active Ingredient Units g/100mL
    Substance Name BENZALKONIUM CHLORIDE
    Labeler Name INDELPA, S.A DE C.V
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH NOT FINAL
    Application Number part333A
    Listing Certified Through 2023-12-31

    Package

    NDC 70697-0804-01 (70697080401)

    NDC Package Code 70697-804-01
    Billing NDC 70697080401
    Package 225 mL in 1 BOTTLE (70697-804-01)
    Marketing Start Date 2020-12-11
    NDC Exclude Flag N
    Pricing Information N/A
    << 70697-0802-01 70697-0805-01 >>

    Contents

    Standard Product Labeling (SPL)/Prescribing Information SPL b62a0129-29de-3a27-e053-2a95a90a7f1a Details

    Revised: 1/2022
    Document Id: d57bdad7-4a59-f656-e053-2a95a90af7b2
    Set id: b62a0129-29de-3a27-e053-2a95a90a7f1a
    Version: 2
    Effective Time: 20220113