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FDA Registration for OTC Oral Health Drug Products

OTC oral health drug products (toothache gels, antiseptic mouthwash, canker sore treatments) are regulated as OTC Monograph drugs by FDA — requiring establishment registration and listing.

OTC MonographDrug Facts Required21 CFR Part 207Since 2009

FDA Requirements for OTC Oral Health Drug Products

OTC oral health drug products include toothache analgesics (benzocaine), antiseptic mouthwashes, and oral wound care products. These are regulated as OTC drugs by FDA.

Note: Cosmetic mouthwashes (breath fresheners only) are cosmetics, not drugs.

  • FDA Drug Establishment Registration
  • NDC Labeler Code
  • Drug Listing with Drug Facts labeling
  • Annual renewal October 1–December 31

The FDA establishes guidelines for over-the-counter (OTC) oral health care drugs through a document called an OTC monograph. This monograph outlines the conditions under which these medications are considered safe and effective for their intended use. Essentially, it sets the standards that OTC oral care products must meet to be sold over the counter without a prescription. The monograph covers various purposes, including pain relief, antiseptic properties, and reduction of plaque and gingivitis. Following this guideline helps ensure that consumers have access to safe and effective oral care products for common concerns.

Oral Health Care Products – Active Ingredients and OTC Monograph Number

M022.12 Anesthetic/analgesics

Active IngredientsOTC Monograph Number
BenzocaineM022.12 (Part 356)
Benzyl alcoholM022.12 (Part 356)
Butacaine sulfateM022.12 (Part 356)
Dyclonine hydrochlorideM022.12 (Part 356)
HexylresorcinolM022.12 (Part 356)
MentholM022.12 (Part 356)
Phenol preparations (phenol and/or phenolate sodium)M022.12 (Part 356)
Salicyl alcoholM022.12 (Part 356)

M022.14 Astringents

Active IngredientsOTC Monograph Number
AlumM022.14 (Part 356)
Zinc chlorideM022.14 (Part 356)

M022.16 Debriding agent/oral wound cleansers

Active IngredientsOTC Monograph Number
Carbamide peroxide in anhydrous glycerinM022.16 (Part 356)
Hydrogen peroxideM022.16 (Part 356)
Sodium bicarbonateM022.16 (Part 356)
Sodium perborate monohydrateM022.16 (Part 356)

M022.18 Demulcents

Active IngredientsOTC Monograph Number
Elm barkM022.18 (Part 356)
GelatinM022.18 (Part 356)
GlycerinM022.18 (Part 356)
PectinM022.18 (Part 356)

M022.20 Oral mucosal protectants

Active IngredientsOTC Monograph Number
Compound benzoin tincture, USP XIXM022.20 (Part 356)
Benzoin tincture, USP XVM022.20 (Part 356)

M022.22 Tooth desensitizers

Active IngredientsOTC Monograph Number
Potassium nitrateM022.22 (Part 356)

These are not complete lists of ingredients in the FDA OTC drug monograph. The status of ingredients in the OTC monograph may change. Please contact the FDA for updated information.

OTC Oral Health Drug Products — FAQs

Common questions about FDA registration requirements for otc oral health drug products.

Mouthwash that makes antiseptic or therapeutic claims (such as reducing plaque or treating gum disease) is classified as an OTC drug. Conversely, products that make only cosmetic claims (such as breath freshening) and contain no active ingredients are regulated as cosmetics.

Yes. Benzocaine-containing toothache gels and oral pain relievers are OTC drugs regulated by FDA.

Ready to Register Your OTC Oral Health Products?

LMG handles drug establishment registration, OTC drug listing, and NDC labeler code for otc oral health products manufacturers worldwide.

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