PREMIERES PAIN

Product NDC: 32472-102
Requested package NDC: 32472-102-01
11-digit product format: 324720102
Labeler code: 32472
Product ID: 32472-102_46a6eefe-da37-067e-e063-6294a90a314c
Type: HUMAN OTC DRUG
Nonproprietary name: menthol
Dosage form: SPRAY
Route: TOPICAL
Labeler: Premiere Enterprises
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2010-12-28
Substance: MENTHOL
Active strength: .07 g/mL
NDC exclude flag: No
Listing certified through: 2027-12-31
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: PREMIERES PAIN
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	.07 g/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1086713	Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
128bd1e7-e961-416c-933b-fbd146e3d386	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
32472-102-01	Premieres Pain	29.5 mL in 1 BOTTLE	SPRAY	29.5	6
32472-102-03	PREMIERES PAIN	88 mL in 1 BOTTLE	SPRAY	88	6
32472-102-04	PREMIERES PAIN	118 mL in 1 BOTTLE	SPRAY	118	6

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
menthol	ACTIVE INGREDIENT	L7T10EIP3A	PREMIERE PAIN ROLL ON (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
menthol	ACTIVE INGREDIENT	L7T10EIP3A	ANALGESIC (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
menthol	ACTIVE INGREDIENT	L7T10EIP3A	PREMIERES PAIN (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
menthol	ACTIVE MOIETY	L7T10EIP3A	ANALGESIC (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
menthol	ACTIVE MOIETY	L7T10EIP3A	PREMIERE PAIN ROLL ON (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
menthol	ACTIVE MOIETY	L7T10EIP3A	PREMIERES PAIN (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
coconut oil	INACTIVE INGREDIENT	Q9L0O73W7L	PREMIERE PAIN ROLL ON (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
coconut oil	INACTIVE INGREDIENT	Q9L0O73W7L	PREMIERES PAIN (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
coconut oil	INACTIVE INGREDIENT	Q9L0O73W7L	ANALGESIC (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
eucalyptus oil	INACTIVE INGREDIENT	2R04ONI662	ANALGESIC (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
eucalyptus oil	INACTIVE INGREDIENT	2R04ONI662	PREMIERES PAIN (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
eucalyptus oil	INACTIVE INGREDIENT	2R04ONI662	PREMIERE PAIN ROLL ON (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
glycerin	INACTIVE INGREDIENT	PDC6A3C0OX	ANALGESIC (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
glycerin	INACTIVE INGREDIENT	PDC6A3C0OX	PREMIERES PAIN (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
glycerin	INACTIVE INGREDIENT	PDC6A3C0OX	PREMIERE PAIN ROLL ON (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
isopropyl alcohol	INACTIVE INGREDIENT	ND2M416302	PREMIERES PAIN (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
isopropyl alcohol	INACTIVE INGREDIENT	ND2M416302	PREMIERE PAIN ROLL ON (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
isopropyl alcohol	INACTIVE INGREDIENT	ND2M416302	ANALGESIC (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
methyl salicylate	INACTIVE INGREDIENT	LAV5U5022Y	ANALGESIC (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
methyl salicylate	INACTIVE INGREDIENT	LAV5U5022Y	PREMIERES PAIN (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
methyl salicylate	INACTIVE INGREDIENT	LAV5U5022Y	PREMIERE PAIN ROLL ON (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
peppermint oil	INACTIVE INGREDIENT	AV092KU4JH	PREMIERE PAIN ROLL ON (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
peppermint oil	INACTIVE INGREDIENT	AV092KU4JH	PREMIERES PAIN (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
peppermint oil	INACTIVE INGREDIENT	AV092KU4JH	ANALGESIC (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
water	INACTIVE INGREDIENT	059QF0KO0R	ANALGESIC (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
water	INACTIVE INGREDIENT	059QF0KO0R	PREMIERE PAIN ROLL ON (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
water	INACTIVE INGREDIENT	059QF0KO0R	PREMIERES PAIN (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2
xanthan gum	INACTIVE INGREDIENT	TTV12P4NEE	PREMIERE PAIN ROLL ON (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
32472-102	PREMIERES PAIN (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	5	Current NDC, Legacy NDC, 1 package rows	20241225_128bd1e7-e961-416c-933b-fbd146e3d386.zip
32472-102	PREMIERES PAIN (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	5	Current NDC, Legacy NDC, 1 package rows	20241225_1f081913-6106-4d06-a37a-631f710dbacb.zip
32472-102	PREMIERES PAIN (MENTHOL) SPRAY [PREMIERE ENTERPRISES]	5	Current NDC, Legacy NDC, 1 package rows	20241225_35ff19df-4cc4-4fce-bd30-d87d835e0e26.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 87 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Good Neighbor Pharmacy Hydrocortisone with Aloe	HYDROCORTISONE	AmerisourceBergen	0c544792-63d9-400c-9888-207c44fdc75e	2025-07-08	Warnings	Exact identifier application number: M017
Good Neighbor Pharmacy Hydrocortisone	HYDROCORTISONE	AmerisourceBergen	58b0b7ba-e547-4e0f-b04d-8e1e6a5d4fcf	2025-07-08	Warnings	Exact identifier application number: M017
Publix Hydro	HYDROCORTISONE	Publix Super Markets Inc	29296b0f-0eed-4bb9-8727-c25c2bcf9fd6	2025-07-08	Warnings	Exact identifier application number: M017
Publix hydro plus	HYDROCORTISONE	Publix Super Markets Inc	a00d82c1-6b09-424a-be78-2603eee3fb9d	2025-07-08	Warnings	Exact identifier application number: M017
Tattoo	TATTOO CREAM	Perfso (HK) Co., Limited	39773cab-12df-4520-e063-6294a90abc5b	2025-07-08	Warnings	Exact identifier application number: M017
Neutrogena Sun Rescue After Sun Medicated Relief	CAMPHOR (SYNTHETIC)	Kenvue Brands LLC	c95c5b64-b90f-1143-e053-2a95a90aa03c	2025-07-07	Warnings	Exact identifier application number: M017
sunmark Hydrocortisone	HYDROCORTISONE	Strategic Sourcing Services LLC	210079e9-3d2f-4489-b468-b96b145034ed	2025-07-07	Warnings	Exact identifier application number: M017
Relief Gel	LIDOCAINE HCL	Good Clean Love, Inc.	e5fa2265-ccb7-750c-e053-2995a90aa51e	2025-07-07	Warnings	Exact identifier application number: M017
Hydrocortisone Plus 12 Moisturizers	HYDROCORTISONE	Sun Pharmaceutical Industries, Inc.	09ac2749-a60f-4039-8c80-a0d2eaf50c34	2025-07-07	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	Sun Pharmaceutical Industries, Inc.	2ada9ec2-1c28-4da2-8639-07b3193ffb32	2025-07-03	Warnings	Exact identifier application number: M017
Hydrocortisone with Aloe	HYDROCORTISONE	Sun Pharmaceutical Industries, Inc.	caa2fd64-e262-4d7c-ad8a-69f506feba8c	2025-07-03	Warnings	Exact identifier application number: M017
Stopain Extra Strength	MENTHOL	Troy Manufacturing, Inc.	07e9a235-6d10-4407-8729-beaf936e97ad	2025-07-03	Warnings	Exact identifier application number: M017
Blue Ice Topical Analgesic Gel	ICE GEL	International Wholesale	397cd306-078d-5b7d-e063-6294a90a8bbc	2025-07-03	Warnings	Exact identifier application number: M017
LIDOCAINE	LIDOCAINE, MENTHOL	Vive Health LLC	236ccc6d-21b7-6153-e063-6394a90a4634	2025-07-02	Warnings	Exact identifier application number: M017
AsperFlex MAX	LIDOCAINE 4% WITH MENTHOL 1%	Akron Pharma Inc.	ccf6172b-350a-4b78-b844-f84bf17c491f	2025-07-02	Warnings	Exact identifier application number: M017
METHYL SALICYLATE 25%	METHYL SALICYLATE	Oncora Pharma, LLC	3766e3a9-94a8-4c3e-e063-6394a90aa24a	2025-07-01	Warnings	Exact identifier application number: M017
Diphenhydramine Hydrochloride and Zinc Acetate	DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE	Sun Pharmaceutical Industries, Inc.	c89e3de8-7d71-485c-8fc5-2832d6024f16	2025-07-01	Warnings	Exact identifier application number: M017
Westlake Outdoor Pain and Itch Relieving	LIDOCAINE 4% PAIN AND ITCH RELIEVING	WESTLAKE HB PHARMA	3c563b28-4f4f-9d0c-e063-6294a90adf73	2025-07-01	Warnings	Exact identifier application number: M017
Cortizone 10 Water Resistant	HYDROCORTISONE	Chattem, Inc.	118e55e7-241f-44c4-959e-09bf6221bd77	2025-07-01	Warnings	Exact identifier application number: M017
Quit Smoking Nicotine Patches	NICOTINE TRANSDERMAL PATCHES	Shenzhen Paxi Trading Co., Ltd.	38c1616e-3b09-0669-e063-6294a90a2c86	2025-06-29	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1086713	menthol 7 % Topical Spray	PSN	128bd1e7-e961-416c-933b-fbd146e3d386	6
1086713	menthol 7 % Topical Spray	PSN	1f081913-6106-4d06-a37a-631f710dbacb	6
1086713	menthol 7 % Topical Spray	PSN	35ff19df-4cc4-4fce-bd30-d87d835e0e26	6
1086713	menthol 70 MG/ML Topical Spray	SCD	128bd1e7-e961-416c-933b-fbd146e3d386	6
1086713	menthol 70 MG/ML Topical Spray	SCD	1f081913-6106-4d06-a37a-631f710dbacb	6
1086713	menthol 70 MG/ML Topical Spray	SCD	35ff19df-4cc4-4fce-bd30-d87d835e0e26	6
1086713	menthol 7 % Topical Spray	SY	128bd1e7-e961-416c-933b-fbd146e3d386	6
1086713	menthol 7 % Topical Spray	SY	1f081913-6106-4d06-a37a-631f710dbacb	6
1086713	menthol 7 % Topical Spray	SY	35ff19df-4cc4-4fce-bd30-d87d835e0e26	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
32472-102-01	32472010201	29.5 mL in 1 BOTTLE (32472-102-01)	29.5 ml	2011-03-07	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
PREMIERE'S PAIN SPRAY	Premiere Enterprises \| Safetec of America, Inc.	2025-12-23	HUMAN OTC DRUG LABEL	6
Analgesic	Premiere Enterprises \| Safetec of America, Inc.	2025-12-23	HUMAN OTC DRUG LABEL	6
PREMIERE'S PAIN SPRAY ROLL-ON	Premiere Enterprises \| Safetec of America, Inc.	2025-12-23	HUMAN OTC DRUG LABEL	6