FDA.reportPublic FDA data

Hush Anesthetic

Product NDC
49947-001
11-digit product format
499470001
Labeler code
49947
Product ID
49947-001_4342d365-43c2-3c5f-e063-6294a90a0dc4
Type
HUMAN OTC DRUG
Nonproprietary name
Lidocaine
Dosage form
SPRAY
Route
TOPICAL
Labeler
HUSH Anesthetic
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2012-12-01
Substance
LIDOCAINE
Active strength
40 mg/g
Pharmacologic classes
Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
Hush Anesthetic
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LIDOCAINE40 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
98PI200987Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1045432Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
c6e86a0f-6f9b-45b7-86ce-0bb1c198061aAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49947-001-02Hush Anesthetic56.7 g in 1 BOTTLE, SPRAYSPRAY56.720
49947-001-04Hush Anesthetic113.4 g in 1 BOTTLE, SPRAYSPRAY113.420

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LIDOCAINEACTIVE INGREDIENT98PI200987HUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]3
LIDOCAINEACTIVE MOIETY98PI200987HUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]3
ALCOHOLINACTIVE INGREDIENT3K9958V90MHUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]3
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0XHUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]3
CALENDULA OFFICINALIS FLOWERINACTIVE INGREDIENTP0M7O4Y7YDHUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]3
CAPRYLYL GLYCOLINACTIVE INGREDIENT00YIU5438UHUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]3
CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)INACTIVE INGREDIENT132584PQMOHUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]3
CHAMAEMELUM NOBILE FLOWERINACTIVE INGREDIENTO2T154T6OGHUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]3
COMFREY ROOTINACTIVE INGREDIENTM9VVZ08EKQHUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]3
EDETATE DISODIUM ANHYDROUSINACTIVE INGREDIENT8NLQ36F6MMHUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]3
GLYCERININACTIVE INGREDIENTPDC6A3C0OXHUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]3
GREEN TEA LEAFINACTIVE INGREDIENTW2ZU1RY8B0HUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]3
MENTHOLINACTIVE INGREDIENTL7T10EIP3AHUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]3
METHYLISOTHIAZOLINONEINACTIVE INGREDIENT229D0E1QFAHUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]3
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3HUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]3
TROLAMINEINACTIVE INGREDIENT9O3K93S3TKHUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]3
WATERINACTIVE INGREDIENT059QF0KO0RHUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49947-001HUSH ANESTHETIC (LIDOCAINE) SPRAY [HUSH ANESTHETIC]8Current NDC, Legacy NDC, 2 package rows20241215_c6e86a0f-6f9b-45b7-86ce-0bb1c198061a.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 9 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
REINREUDE BACK PAIN THERAPYCAMPHOR 80MG MENTHOL 24MG BACK PAIN THERAPYJiangxi Yudexi Pharmaceutical Co., LTD4dfc77bb-11dd-e0f0-e063-6294a90a4e9c2026-07-24WarningsExact identifier
application number: M017
DRAVYNOR QUIT SMOKING PatchesNICOTINE18% MENTHOL 0.3% QUIT SMOKING PATCHESWenzhou Yuyuan Pharmaceutical Co., Ltd.5768631f-d517-5b43-e063-6294a90a8f462026-07-24WarningsExact identifier
application number: M017
DERMFREE NUMBINGLIDOCAINE4% NUMBINGJiangxi Yudexi Pharmaceutical Co., LTD4a5b47ce-2bf1-42c7-e063-6294a90af09f2026-07-23WarningsExact identifier
application number: M017
DERMFREE WART CORN REMOVERSALICYLIC ACID 40% WART CORN REMOVERJiangxi Yudexi Pharmaceutical Co., LTD4a5c63b3-44de-8736-e063-6394a90ac21a2026-07-23WarningsExact identifier
application number: M017
DERMFREE Anti-itchHYDROCORTISONE1% ANTI-ITCHJiangxi Yudexi Pharmaceutical Co., LTD4a5af4c6-555a-e74c-e063-6394a90aa6ce2026-07-23WarningsExact identifier
application number: M017
DERMFREE HEMORRHOIDLIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOIDJiangxi Yudexi Pharmaceutical Co., LTD4a5d0e79-d620-0147-e063-6294a90a31032026-07-23WarningsExact identifier
application number: M017
MAG 5 PT WARMING FORMULAMENTHOLRENU LABORATORIES, LLCa499ac9b-0e8e-e23f-e053-2a95a90abe9a2026-07-23WarningsExact identifier
application number: M017
Icy Hot Performance Cream Pain ReliefMENTHOL 16%, CAMPHOR 11%Chattem, Inc.73f7a113-ef11-4932-bf4d-4e62863f79412026-07-23WarningsExact identifier
application number: M017
Numbing Pain ReliefLIDOCAINE 4%Walgreen Company2425badb-e196-e9f8-e063-6294a90a7bf42026-07-22WarningsExact identifier
application number: M017
Cooling Pain ReliefMENTHOL 4.5%Walgreen Company24345ccf-c96f-31b0-e063-6294a90a82b52026-07-22WarningsExact identifier
application number: M017
Heat Pain ReliefCAPSAICIN 0.1%Walgreen Company2434f9cf-74aa-17af-e063-6294a90a56d92026-07-22WarningsExact identifier
application number: M017
Pain Relief Patch LidocaineLIDOCAINEHyVee41c26a66-3371-2c2c-e063-6294a90aa38b2026-07-22WarningsExact identifier
application number: M017
CVS Ultra Strength MuscleMENTHOL, CAMPHOR, METHYL SALICYLATECVS Pharmacy48bef8bc-6e39-a328-e063-6394a90ae4502026-07-22WarningsExact identifier
application number: M017
HydrocortisoneHYDROCORTISONEAKRON PHARMA INCdaad9a1e-98d2-4ce7-9d97-ac5d81905abb2026-07-22WarningsExact identifier
application number: M017
Professional Therapy MuscleCare Pain RelievingMENTHOL, CAMPHORActive and Innovative573c2d85-9e0b-7955-e063-6394a90aff642026-07-22WarningsExact identifier
application number: M017
DOCTOR INK TOPICAL ANTISEPTIC WITH PAIN RELIEFBENZALKONIUM CHLORIDE, LIDOCAINEEnviro Specialty Chemicals Incf7abe66c-dc2d-4ef7-9b11-5b87157fd3022026-07-21WarningsExact identifier
application number: M017
Bclsks NUMBINGMENTHOL 1% NUMBINGJiangxi Yudexi Pharmaceutical Co., LTD49e26770-ddf6-7515-e063-6394a90a4ab32026-07-21WarningsExact identifier
application number: M017
Rstrvbr QUIT SMOKINGNICOTINE21MG QUIT SMOKINGJiangxi Yudexi Pharmaceutical Co., LTD4a5e9691-727f-6bcd-e063-6294a90aadfc2026-07-21WarningsExact identifier
application number: M017
Rstrvbr QUIT SMOKINGNICOTINE14MG QUIT SMOKINGJiangxi Yudexi Pharmaceutical Co., LTD4a5eec19-7f9a-d277-e063-6294a90ace952026-07-21WarningsExact identifier
application number: M017
Rstrvbr QUIT SMOKINGNICOTINE7MG QUIT SMOKINGJiangxi Yudexi Pharmaceutical Co., LTD4a5f124e-2dd7-16b8-e063-6294a90a5cdb2026-07-21WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1045432lidocaine HCl 4 % Topical SprayPSNc6e86a0f-6f9b-45b7-86ce-0bb1c198061a20
1045432lidocaine hydrochloride 40 MG/ML Topical SpraySCDc6e86a0f-6f9b-45b7-86ce-0bb1c198061a20
1045432lidocaine HCl 4 % Topical SpraySYc6e86a0f-6f9b-45b7-86ce-0bb1c198061a20
1045432lidocaine HCl 4 % Topical Spray GelSYc6e86a0f-6f9b-45b7-86ce-0bb1c198061a20

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49947-001-024994700010256.7 g in 1 BOTTLE, SPRAY (49947-001-02) 56.7 g2012-12-010000-00-00NoNoCurrent
49947-001-0449947000104113.4 g in 1 BOTTLE, SPRAY (49947-001-04) 113.4 g2012-12-010000-00-00NoNoCurrent