65517-1002 : Dawnmist Antiperspirant Deodorant 79 mg/ml Topical Liquid


NDC: 65517-1002
Labeler: Dukal Corporation
Product Type: Human OTC Drug
Drug Name: Dawnmist Antiperspirant Deodorant
Dosage Form: Topical Liquid
Application #: part350
Rev. Date: 


NDC Package Codes:

  • 65517-1002-1: 59 ML IN 1 BOTTLE, PUMP (65517‑1002‑1)
  • 65517-1002-2: 118 ML IN 1 BOTTLE, PUMP (65517‑1002‑2)

Active Ingredients:

  • Aluminum Chlorohydrate

Dosage Strength:

  • 79 mg/mL

Related Products:

Based on records with the same trade name.
  • 65517-1004 Dawnmist Antiperspirant Deodorant 45 mg/ml Topical Liquid by Dukal Corporation
  • 65517-1005 Dawnmist Antiperspirant Deodorant 45 mg/ml Topical Liquid by Dukal Corporation
  • 65517-1008 Dawnmist Antiperspirant Deodorant 45 mg/ml Topical Liquid by Dukal Corporation
  • 65517-1009 Dawnmist Antiperspirant Deodorant 45 mg/ml Topical Liquid by Dukal Corporation
  • 65517-1010 Dawnmist Antiperspirant Deodorant 78 mg/ml Topical Liquid by Dukal Corporation
  • 65517-1011 Dawnmist Antiperspirant Deodorant 78 mg/ml Topical Liquid by Dukal Corporation
  • 65517-1014 Dawnmist Antiperspirant Deodorant 45 mg/ml Topical Gel by Dukal Corporation
  • 65517-1015 Dawnmist Antiperspirant Deodorant 150 mg/ml Topical Gel by Dukal Corporation
  • 65517-1021 Dawnmist Antiperspirant Deodorant 78 mg/ml Topical Lotion by Dukal Corporation

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.