FDA.report

Tampax

Primary DI
40073010021431
Brand
Tampax
Company
PROCTER & GAMBLE MANUFACTURING COMPANY, THE
Model
Tampax Radiant
Device description
TAMPAX RADIANT REGULAR 32CT
Published
2016-09-15
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
false
Single use
true

Related Records

Product Codes

CodeName
HEBTAMPON, MENSTRUAL, UNSCENTED

Product Code Classifications

CodeDeviceSpecialtyClass
HEBTampon, Menstrual, UnscentedObstetrics/Gynecology2

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00073010021938PackageGS16In Commercial Distribution
10073010021430PackageGS16In Commercial Distribution
40073010021431PackageGS190In Commercial Distribution
40073010021936PackageGS190In Commercial Distribution
00073010021433PrimaryGS10
50073010021438Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00073010021938000730100219380730100219380073010021938
1007301002143010073010021430
4007301002143140073010021431
4007301002193640073010021936
00073010021433000730100214330730100214330073010021433
5007301002143850073010021438

GMDN Terms

TermDefinition
Menstrual tampon, unscentedA non-sterile, non-deodorized plug made of cellulosic or synthetic material that is inserted into the vagina to absorb menstrual or other vaginal discharge. This is a single-use device.

Sterilization Methods

Method

Regulatory Flags

DUNS number
004238200
Device count
32
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

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