ANTIPAIN-S

Manufacturer: GEORGE L. RODRIGUEZ M.D., PC
Effective date: 2014-08-12
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:06:10

Label at a glance#

ProductANTIPAIN-S

Active ingredientCLEMATIS HEXAPETALA WHOLE, MOMORDICA CHARANTIA WHOLE, MYRRH, FRANKINCENSE OIL, MENTHOL

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

CONTENTS:

EACH 1.0 GM CONTAINS:

RADIX CLEMENTIS.....30 MG

YELLOW WAX.....30 MG

SEMEN MOMORDICAE.....15 MG

SEMEN RICINI.....50 MG

MYRRHA.....20 MG

OLIBANUM.....20 MG

MENTHOL.....50 MG

METHYL SALICYLATE.....10 MG

OTC - PURPOSE SECTION

PURPOSE

PAIN RELIEF

WARNINGS SECTION

CAUTIONS:

DO NOT USE THIS PRODUCT IF YOU HAVE A SENSITIVE SKIN.

DO NOT APPLY TO THE WOUNDED OR DAMAGED SKIN.

AVOID EYE CONTACT.

DISCONTINUE USE IF SIGNS OF IRRITATION APPEAR. IF IRRITATION PERSISTS, CONSULT A DOCTOR. IF YOU ARE ALLERGIC TO ANY INGREDIENT IN THE PRODUCT, DO NOT USE.

INDICATIONS & USAGE SECTION

RELIEVING SWELLING AND PAIN OF TRAUMA OR FRACTURE. RELIEVING THE PAIN OF LIMBS, SHOULDER AND BACK. RELIEVNG THE PAIN DUE TO DAMP AND CHILL.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS:

FOR EXTERNAL USE ONLY.

CLEAN THE UNCOMFORTABLE AREAS BEFORE APPLY. 3-4 TIMES PER DAY.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

INACTIVE INGREDIENT SECTION

YELLOW WAX.....30 MG

SEMEN RICINI.....50 MG

PETROLATUM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ointment Box

Ointment Tube Front

Ointment Tube Back

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69165-201-51	2020-01-31	C162847	48780-1	9d75b9d0-e9dd-f424-e053-dadaa90a57ce	04693391-894e-4853-a0c8-9eb304e63313

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69165-201-21	ANTIPAIN-S	35 g in 1 TUBE	OINTMENT	35		1
69165-201-51	ANTIPAIN-S	1 in 1 BOX	OINTMENT	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69165-201	ANTIPAIN-S (RADIX CLEMATIDIS, SEMEN MOMORDICAE, MYRRHA, OLIBANUM, MENTHOL, METHYL SALICYLATE) OINTMENT [GEORGE L. RODRIGUEZ M.D., PC]	1	Legacy NDC, 2 package rows	20141117_04693391-894e-4853-a0c8-9eb304e63313.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
CLEMATIS HEXAPETALA WHOLE	ACTIVE INGREDIENT	8F900R77RS	1
FRANKINCENSE OIL	ACTIVE INGREDIENT	67ZYA5T02K	1
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	1
MOMORDICA CHARANTIA WHOLE	ACTIVE INGREDIENT	83M15WOS0F	1
MYRRH	ACTIVE INGREDIENT	JC71GJ1F3L	1
CLEMATIS HEXAPETALA WHOLE	ACTIVE MOIETY	8F900R77RS	1
FRANKINCENSE OIL	ACTIVE MOIETY	67ZYA5T02K	1
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	1
MOMORDICA CHARANTIA WHOLE	ACTIVE MOIETY	83M15WOS0F	1
MYRRH	ACTIVE MOIETY	JC71GJ1F3L	1
PETROLATUM	INACTIVE INGREDIENT	4T6H12BN9U	1
RICINUS COMMUNIS WHOLE	INACTIVE INGREDIENT	Q94QWM85RF	1
YELLOW WAX	INACTIVE INGREDIENT	2ZA36H0S2V	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

ANTIPAIN-S
RADIX CLEMATIDIS, SEMEN MOMORDICAE, MYRRHA, OLIBANUM, MENTHOL, METHYL SALICYLATE
CLEMATIS HEXAPETALA WHOLE
YELLOW WAX
MOMORDICA CHARANTIA WHOLE
RICINUS COMMUNIS WHOLE
MYRRH
FRANKINCENSE OIL
MENTHOL
PETROLATUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69165-201	69165-201-21, 69165-201-51

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CLEMATIS HEXAPETALA WHOLE	8F900R77RS	ACTIB
YELLOW WAX	2ZA36H0S2V	IACT
MOMORDICA CHARANTIA WHOLE	83M15WOS0F	ACTIB
RICINUS COMMUNIS WHOLE	Q94QWM85RF	IACT
MYRRH	JC71GJ1F3L	ACTIB
FRANKINCENSE OIL	67ZYA5T02K	ACTIB
MENTHOL	L7T10EIP3A	ACTIB
PETROLATUM	4T6H12BN9U	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 27 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
PETROLATUM	PETROLATUM	4T6H12BN9U	AEROSOL, FOAM / TOPICAL	7.9 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	TABLET / ORAL	3.5 mg		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	CREAM / TOPICAL		4213 mg	Exact identifier — unii candidate 18 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	TABLET, EXTENDED RELEASE / ORAL	0.01 mg		Exact identifier — unii candidate 9 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	CAPSULE, EXTENDED RELEASE / ORAL	0.07 mg		Exact identifier — unii candidate 18 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	TABLET, DELAYED RELEASE / ORAL	0.1 mg		Exact identifier — unii candidate 9 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	OINTMENT / VAGINAL		4084 mg	Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	SPONGE / TOPICAL	NA		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	OINTMENT / OPHTHALMIC	88.4 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	TABLET, EXTENDED RELEASE / ORAL	0.18 mg		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	LOTION / TOPICAL	25 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	SUPPOSITORY / VAGINAL	27 mg		Exact identifier — unii candidate 18 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	CAPSULE / ORAL		44 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	CREAM, AUGMENTED / TOPICAL	26 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	LIQUID / RESPIRATORY (INHALATION)	NA		Exact identifier — unii candidate 18 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	CAPSULE, EXTENDED RELEASE / ORAL	80.67 mg		Exact identifier — unii candidate 9 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	EMULSION / TOPICAL	7.8 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	OINTMENT / TOPICAL	20 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	TABLET / ORAL	3.22 mg		Exact identifier — unii candidate 9 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	TABLET, SUGAR COATED / ORAL	NA		Exact identifier — unii candidate 9 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	OINTMENT / AURICULAR (OTIC)	NA		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	SOAP / TOPICAL	0.85 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	CAPSULE / VAGINAL	NA		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	OINTMENT, AUGMENTED / TOPICAL	81.94 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	OINTMENT / TOPICAL		7275 mg	Exact identifier — unii candidate 18 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	CREAM / TOPICAL	5 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	TABLET, COATED / ORAL	213.7 mg		Exact identifier — unii candidate 9 equally ranked IID candidates

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f50769ca-2c0d-422d-91ea-1c37b5a64b4c			04693391-894e-4853-a0c8-9eb304e63313	2014-08-12	Warnings	Exact identifier spl id: f50769ca-2c0d-422d-91ea-1c37b5a64b4c spl set id: 04693391-894e-4853-a0c8-9eb304e63313

Reported adverse events (FAERS/openFDA)#

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